Take part in research
In this section, you will find a list of all clinical research studies currently being supported by our department.
Research studies by category (A-Z)
Anxiety and Depression
The GLAD Study is a project set up to explore risk factors in individuals who have experienced depression and/or anxiety, including those with a diagnosis of bipolar disorder, OCD, or related disorders, at any time in their lives.
It aims to better understand depression and anxiety in order to find and develop more effective treatments. The GLAD Study is also part of the NIHR BioResource, which is a library of information about people’s health aiming to support research in both physical and mental health.
To take part in this study, people must:
- Have experienced symptoms of anxiety and/or depression during their life, or have never experienced any mental health condition
- Be aged 16 and above
- Live in the UK
The GLAD Study enrolment process consists of four steps:
- Register on the website www.gladstudy.org.uk and read the Information Sheet
- Provide consent (please put AWP as where you heard about the study)
- Complete a questionnaire
- Provide a saliva sample
AWP Research and Development contacts:
Alexandra Young (alexandra
This study will close on the 01 November 2028
Background
This Social Brain Study looks at how different people seeking support for various mental health difficulties such as anxiety and depression-related problems, behave in social interactions.
The study aims to address some of the current gaps in knowledge and investigate whether there is a relationship between mental health difficulties and social interactions and if so, whether social behaviours can be predicted or modelled using personality/character traits.
This will hopefully improve understanding of mental health difficulties and contribute toward developing more informed and effective treatments.
To take part in this study, people must be:
- On a waiting list for high intensity / step 3 Talking Therapy provided by the Avon and Wiltshire Mental Health Partnership NHS Trust
- Aged 18-60
- Able to read and write in English
- Not have a primary diagnosis of a personality, psychotic, or bipolar disorder
Further information:
The University College London is supporting interested AWP service users to take part in the study.
All parts of the study are completed online using the internet.
Participants interested in taking part are asked to complete a short virtual computer game that investigates social interaction/ behaviour and takes around 30 minutes. Participants are also asked to complete a series of self-report questionnaires covering a range of different topics.
Participants will be asked to complete this part of the study in their own time over a 2-3 week period, whilst waiting to start their therapy.
The study also involves a follow up part, which will commence once a participant has started therapy. During this follow up stage, participants are asked to complete 2 short questionnaires every 2 weeks, that take around 5 minutes each.
The Social Brain Study is offering participants a £35 payment at the end of the study as a thank you.
AWP Research and Development contacts:
Darren French, Research Nurse (d
Thalia Pilcher, Research Practitioner (t
This study will close to new applicants on the 31 December 2024.
Bipolar and Psychosis
Attention-Deficit Hyperactivity Disorder (ADHD) is a neurodevelopmental disorder, which involves inattention, hyperactivity and impulsivity. ADHD starts in childhood and often continues into adulthood. ADHD in adults commonly occurs alongside bipolar disorder or psychosis.
ADHD is typically treated with stimulant and non-stimulant medications. The National Institute for Health and Care Excellence (NICE) ADHD guidelines recommend the stimulants, Lisdexamfetamine or Methylphenidate as first line medications. These medications are more effective than the non-stimulant medication, Atomoxetine.
The longer term effects of ADHD medications on those with co-occurring bipolar disorder or psychosis are not well understood.
The SNAPPER study aims to evaluate the clinical and cost effectiveness of the stimulant Lisdexamfetamine compared with non-stimulant Atomoxetine, as medication for adults with ADHD and a history of either psychosis or bipolar disorder.
To take part in this study people must:
- Be aged 18 years or above
- Have a diagnosis of ADHD
- Have a diagnosis of psychosis or bipolar disorder
- Be taking mood stabilisers or anti-psychotics and stable on these medications
- Not currently be taking medication for ADHD, or having been on ADHD medication within the past month
- Be able and willing to give informed consent to take part in the trial
People will be unable to take part in this study if they:
- Are taking part in another interventional or conflicting clinical trial
- Are experiencing an acute episode of psychosis or bipolar disorder
- Are at severe risk of suicide and/or violence to others
- Have severe drug seeking behaviour or current drug or alcohol withdrawal syndrome
- Have a history of epilepsy or seizures
- Have Congenital or acquired long QT syndrome (LQTS) or a family history of QT prolongation
- Are taking medication which can increase risk of QT interval prolongation, including anti-arrhythmics, moxifloxacin, erythromycin, methadone, mefloquine, tricyclic antidepressants or cisapride
- Are taking CYP2D6 inhibitors, for example quinidine or terbinafine
- Are pregnant, as checked with a spot urine test
- Would be unwilling to take highly effective contraception measures to prevent pregnancy during the study period and for 30 day after administration of the last trial medication dose
Further information:
People interested in taking part in this trial will first go through a screening process to ensure that they meet the eligibility criteria to take part in the main trial. This screening process will include health related questions and confirmation of ADHD diagnosis.
If eligible to take part in the main trial, people are invited to give informed consent. Once consented, researchers will ask them further questions about their health using interviews and self-reported questionnaires. This process could take 2 to 3 hours to complete, after which people taking part are randomly allocated to receive either Lisdexamfetamine or Atomoxetine. This medication would be taken for 12 months, which a doctor would regularly prescribe.
People in the trial will have regular medication monitoring with their care team throughout the trial.
The research team would meet with individuals at 3, 6, 9 and 12 months into the trial. These visits will last around an hour. During these visits, those taking part will be asked to repeat some of the interviews and self-reported questionnaires that they completed at the start of the trial.
The research team will give those taking part £25 as a thank you for their time and support after completing the first visit, and then again at 6 and 12 month visits.
AWP contact information:
Mashal Asif and Darren French (awp
This study closes on the 31 May 2026
When somebody with bipolar disorder experiences depression, it can be difficult to treat. Depression in bipolar disorder responds differently to psychological interventions than depression in people who have never experienced mania or hypomania. Currently there is limited evidence for the use of antidepressants in bipolar disorder.
The ASCEnD study aims to understand whether the combination of the antipsychotic aripiprazole and an antidepressant called sertraline will improve symptoms of depression in adults with bipolar.
To take part people must:
- Be aged 18 or above
- Be an Avon and Wiltshire Mental Health Partnership NHS Trust service user
- Have a diagnosis of a depressive episode within bipolar disorder
- Be uncertain of their next course of medication treatment
- Not have a severe substance use disorder
Further information:
Participating in the study will last up to 24 weeks. Participants will be randomly allocated (like tossing a coin) to receive either a combination sertraline/aripiprazole combination or the antipsychotic quetiapine. Participants will be supported by a study doctor during this time period.
At the beginning of the study, participants will attend an appointment with the local research team to discuss the study and eligibility to take part. This meeting will also involve completion of some questionnaires about the participant and their health.
Participants will then complete weekly online questionnaires at home about their mood and quality of live during the 24 weeks of the study. Participants will also receive a weekly phone call from a study research assistant to discuss mood, behaviours, symptoms, and medication.
Some participants will have the opportunity to be interviewed about their experiences of taking part in the study.
Participants who are eligible for the study will receive a £15 voucher at the initial study appointment, a £20 voucher at week 14 of the study, and another £15 voucher upon completion of participation in the study to thank them for their time.
Contact details:
If you have any questions or would like further information please contact a member of the AWP Research and Development team at the following email address:
This study closes on the 31 August 2025
The Integrated Bipolar Parenting Intervention Trial (IBPI) team based at Lancaster University and Lancashire and South Cumbria NHS Foundation Trust are trying to find out whether providing online parenting support for parents with bipolar disorder (BD) helps parents to feel less stressed, have more confidence and experience fewer mood problems. The trial also aims to see whether use of the support leads their children to having fewer behavioural and emotional problems.
To take part in this trial, people must:
- Have a diagnosis of Bipolar Disorder (BD)
- Have a child aged 4-10 years old (with whom you have at least 10 hours of contact with a week)
- Have access to the internet
Further Information:
The Integrated Bipolar Parenting Intervention (IBPI) is an online tool that combines parenting support with helpful strategies for managing bipolar, and can be accessed on computers, mobile phones or tablets.
Individuals will be randomly allocated (50/50 chance) to receive the intervention or to receive what would be considered their usual care. Those that are allocated to receive usual care will be able to access the IBPI tool once they have completed the trial (after 48 weeks).
All activities related to the IBPI Trial will be done remotely / online.
If you are interested in finding out more and registering your interest, please visit: Bipolar-Parenting-Study | Lancaster University
IBPI Trial contact:
Telephone: 07507 856960
Email: ibpi
Website: www.lancs.ac.uk/spectrum/IBPI
This study will close on the 31 January 2025
Some people feel worried and concerned that others are trying to harm them. This can lead to people feeling unsafe and not doing the activities they enjoy. Feeling Safer is a new guided online therapy programme. It is designed to help people feel safer, happier, and get back to doing more of the things they want to be doing.
This study aims to find out whether the Feeling Safer programme can help people to feel less worried that other people are going to harm them. The study will also explore if Feeling Safer leads to other improvements in people’s lives. For example, activity levels, anxiety and quality of life.
To take part, people must:
- Be age 16 or over
- Have strong beliefs and worries that someone is trying to harm them in some way
- Be attending mental health services within AWP for a diagnosis of psychosis
Further information:
Eligible people who want to take part will be randomly placed into groups. We need some participants to continue with their usual care. This is so that we can work out how effective Feeling Safer is compared to usual treatment. This means the following:
- three quarters of participants will receive Feeling Safer as well as continuing with their usual treatment
- a quarter of participants will only receive their usual treatment
People receiving Feeling Safer will access it using an online program.
If people do not have a suitable device to access the Feeling Safer program, one can be provided for the study.
People will be expected to log into the Feeling Safer program two or three times a week for about 20 minutes.
The therapy is individualised. This means people can choose which parts of the programme they want to do. Possible topics include how to improve sleep or feel more self-confident.
People receiving Feeling Safer will be allocated a trained staff member who will guide and support them through the therapy.
Another study aim is to check that the therapy works well when delivered by different staff professions.
People receiving Feeling Safer will be randomly allocated support from:
- a clinical psychologist
- a lived experience researcher
- a graduate mental health worker, such as an assistant psychologist
All participants will be asked to meet with a research assistant to assess how they are getting on with the study. These assessments take place at the beginning of the study, then after 3, 6 and 9 months. Participation in the study will last about 9 months.
Participants will be offered £15 for each assessment they complete, as a thank you for their time. There are four assessments in the study, so the total thank you per participant is £60.
AWP contact information:
Research coordinators:
Joanna Morris-Bone
Monalisa Bora-White
Research Assistants:
Alicia Ladbrook
Hollie Hymas
Email: awp.feelingsafertrial@nhs.net
This study closes on the 31 January 2026
Psychotic disorders, including Schizophrenia affect many people. Evidence suggests that inflammation in the body may have a role in the development of psychotic symptoms and may make it difficult for people to get better despite taking anti-psychotic medication.
This study aims to examine the role of inflammation in psychosis. To test this, participants who have inflammation will be randomly allocated to receive either the study intervention which is a single Intravenous (IV) infusion of an anti-inflammatory medication which already exists called Tocilizumab or the study control, which is a single IV infusion of normal saline solution which will have no effect on levels of inflammation in the body. Participants will not know whether they have received the intervention or control.
The study will examine if reducing levels of inflammation using the medication can help reduce symptoms of psychosis.
This study will support us to understand whether inflammation has a role in causing psychosis and if in the future, anti-inflammatory drugs may help in the treatment of psychosis for some people.
To take part in this study, people must be:
- Aged 18 - 40
- Diagnosis of psychosis (Schizophrenia or related psychoses) and within three years of first diagnosis of psychotic disorder.
- If on anti-psychotic medication, stable on treatment regime with no changes in the past 2 weeks.
- Able to give informed consent, including consent to share information with your General Practitioner (GP) and to access secondary care and GP records.
- Able to understand written and spoken English.
- Able to consent to providing blood samples.
- Willing to abstain from strenuous exercise for 72 hours before the assessment visits.
- Not pregnant (confirmed by urine pregnancy test) or breast-feeding.
- Have a Body mass index (BMI) < 35 (i.e., WHO obesity class II or below).
- There are other study eligibility criteria, which includes a number of co-morbid physical and mental health conditions and history, which are not listed above. If you have any questions about the criteria specifically, please email awp
.pimsresearchtrial .@nhs.net
Further information:
Service users interested in taking part in the trial will be invited to attend a couple of in person appointments. During these appointments, service users will be provided with information about the study, be asked to provide informed consent and will be assessed for suitability for the trial. During these appointments, service users will complete some questionnaires, cognitive tests and provide blood samples. (There is also an optional MRI scan).
Participants with evidence of inflammation (measured by a blood test), will also be asked to complete some further blood tests and a chest X-Ray before being randomised into the study.
Participants with no evidence of inflammation, will stop taking part in the study at this stage.
Participants who have of psychosis and inflammation who are eligible to take part in the trial, will be randomised to receive either a single dose of Tocilizumab or normal saline solution, which are administered via intravenous (IV) infusion.
The study also involves some follow up appointments at 7 days, 14 days and 28 days after receiving the infusion. During these appointments, participants are asked to complete further blood tests, questionnaires and cognitive tests (there is also an optional MRI scan).
Participation in the trial will end at 42 days after receiving the infusion when participants are contacted by the study team for a final check in.
Eligible service users who take part in the trial will be offered payment after completing different stages of the study, as a thank you for their time.
Participants can also claim reimbursement for travel expenses.
The PIMS Trial study website: Psychosis Immune Mechanism Stratified Medicine Study - University of Birmingham
AWP Research and Development contacts:
If you wish to discuss the PIMS Trial or are interested in taking part in the study, you can contact the PIMS study team by email awp
This study will close on the 15 February 2025.
Many people attending mental health services have difficulties sleeping.
Difficulties sleeping could include the following:
- Lying in bed for hours without sleep
- Having nightmares
- Being up all night because of fears or hearing voices
- Sleeping a lot in the day
- Having very irregular sleep patterns and sleeping at the wrong times
This study aims to find out if an eight-session sleep therapy can improve sleep compared to support available routinely on the NHS.
The study team also want to find out whether improving sleep brings other benefits to a person’s life. For example, if it improves mood, concentration, and thinking.
To take part in this study, people must be:
- Aged 16 years and above who have difficulties sleeping, and who are attending NHS mental health services for conditions such as psychosis
OR
- Aged 14 years and above who have difficulties sleeping, and who are attending NHS mental health services for other difficulties such as worries about other people or hearing voices
Further information:
Everyone eligible and who choose to take part will be asked to meet with a research assistant for an assessment at the start of the study. Following this assessment the person will be randomly allocated to receive either the sleep therapy or the normal treatment available through their care team.
There are two further assessments, one at 12 weeks and the other at 24 weeks into the study. Each assessment involves completing questionnaires and answering questions with a researcher, which can last up to 3 hours each time. People taking part would be welcome to take breaks when needed or complete each assessment over several meetings to reduce fatigue.
Participation in the study lasts about six monthly in total. If people are allocated to receive the sleep therapy, it involves eight sessions over twelve weeks.
People taking part will receive £15 for each of the three assessment sessions they take part in. If all three assessment sessions are completed this will be a total of £45. The study team will also reimburse any reasonable travel costs for attending the assessments.
AWP contact information:
awp
This study closes on the 31 December 2026
Some people with bipolar disorder experience ongoing low mood or mood swings outside of episodes of depression or mania. There is not yet a therapy designed to address these ongoing symptoms.
The University of Exeter is currently running a study testing a new talking therapy they have developed for people who have ongoing symptoms of bipolar disorder between major episodes. The findings of this study will help the study team to plan for a larger, future trial of the therapy that will be able to say whether or not it would be a helpful addition to the care that is currently available in the NHS for people with ongoing bipolar symptoms.
To take part in this study, people must:
- Be aged 18 or over
- Meet diagnostic criteria for Bipolar I or II Disorder, Other Specified Bipolar Disorder, or Cyclothymic Disorder
- Not currently be experiencing a manic or severe depressive episode
- Currently experiencing inter-episode bipolar symptoms
- Be willing to engage in psychological work addressing inter-episode bipolar symptoms
- Have an understanding of written and spoken English
- Be registered with a General Practitioner within the Avon and Wiltshire Mental Health Partnership NHS Trust catchment
- Have no current substance dependence
- Not be receiving another psychological therapy for bipolar disorder
If you have any questions about the criteria for this study please email awp
Further information:
Taking part in this study will involve an initial screening telephone or video call with a member of AWP’s research team to check eligibility. This call will take around 20 minutes. People who may be eligible to take part will then be asked to attend a baseline assessment in person at an AWP site. This assessment will take around 2 to 3 hours.
STABILISE is a randomised control trial, this means eligible people will be allocated randomly (50/50 chance) to receive either the STABILISE talking therapy or treatment-as-usual.
The STABILISE talking therapy is a behavioural therapy designed to support people experiencing ongoing inter-episode bipolar symptoms. This will involve up to 22 individual therapy sessions delivered face-to-face, online, or by phone.
Everyone who takes part in the study will be asked to complete sets of questionnaires at 3, 7, and 12 months after starting the study. Participants will be able to receive a £20 thank you payment for completing the baseline assessment and each of the three follow-up assessment. This would mean a total of £80 for completing all assessments.
Contact information:
Chief Investigator, Dr Kim Wright: (K
Study website: https://www.exeter.ac.uk/research/mooddisorders/research/currentprojects/stabilise/
Click here to link the a video of the study participant information sheet
This study closes on the 30 June 2025
Background:
The study is aiming to test/validate a new scale that has been developed to measure self-dehumanisation in a clinical sample of people with psychosis. Self-dehumanisation is the feeling that oneself is less than human.
To take part in this trial you must:
- Be aged 18 or older
- Have a diagnosis of schizophrenia spectrum disorder or eligibility for early intervention in psychosis services OR people with experience of distressing psychosis (confirmed by a brief video call).
- Have sufficient fluency in English in order to understand the questions
Additional Information:
Individuals will be asked to complete a number of short questionnaires, supported by a trained member of staff. It is expected that this will take 10 – 15 minutes. Participants will then be asked to complete one of the questionnaires again, 3 days later.
After the study, participants will be debriefed about the purpose and implications of the study. A trained member of staff will be available to talk and answer any questions that the participant might have.
AWP Research and Development contacts:
Monalisa Bora-White (monalisa
Thalia Pilcher (t
This study will close on the 31 January 2025
Visual hallucinations can be distressing and have a negative impact on people’s lives. There is little research into how visual hallucinations are experienced by those with non-affective psychosis.
The VISION-QUEST study aims to develop and test a new questionnaire to understand people’s beliefs about visual hallucinations. This questionnaire will also explore some physical and psychological factors thought to influence visual hallucinations.
To take part in this study, individuals must:
- Be aged 16 years or above
- Be diagnosed with non-affective psychosis; including schizophrenia, schizoaffective disorder, delusional disorder, psychosis not otherwise specified
- Be experiencing visual hallucinations within last month
- Be currently accessing NHS adult secondary
- Be willing and able to give informed consent
Individuals will not be able to take part in this study if they have:
- Insufficient English language to understand and complete questionnaires
- Visions as a result of organic disorder or brain injury, or when only under the influence of substances
Further information:
Those that take part will be asked to complete a questionnaire pack, which should take 30-45mins to complete. This pack can be completed either online or face-to-face with a researcher.
A payment of £10 or equivalent in shopping vouchers will be offered as a thank you for taking part in the study.
A small group that take part will also have the option to complete a similar questionnaire one week later. These questionnaires will take around 15 minutes to complete. These follow-up questionnaires will allow researchers to assess the new measure for visual hallucinations, which is being developed.
A second payment of £10 or equivalent shopping voucher will be offered as a thank you for completing the follow-up part of the study.
Contact:
This study closes on the 4 March 2025
Complex Emotional Needs
Background
For individuals with complex emotional needs (CEN), the support they receive from friends and family can be an important factor on how they manage their recovery. Caring for someone with CEN can be difficult and most carers do not receive information or support from mental health services.
There is some evidence that a group intervention, which is aimed at individuals who care for people with CEN, can benefit service users and their carers in terms of health, wellbeing and resilience.
It is hoped that this small-scale trial will confirm the benefits of the cares group intervention, and that conducting a larger trial would be possible. The findings can be used to make a case for continuing to offer the intervention locally and make a case for a larger multi-site study.
To take part in this study both the service user and their carer / supporter must agree, and consent, to take part.
Inclusion criteria for carers:
- Be aged 18 or above
- Be identified as a carer or supporter for a person with complex emotional needs by a service user, a clinician or by themselves
- Be willing to attend a series of carer intervention groups
- Be able and willing to provide written informed consent to take part
- Have access to Personal Computer, laptop, or smartphone and good quality internet for the purpose of completing the intervention sessions, questionnaires and any research interviews online
- Have not attended and completed the carer group intervention sessions previously
Inclusion criteria for service users:
- Be aged 18 or above
- Be presenting with complex emotional needs and severe emotion dysregulation, and/or a clinical diagnosis of Borderline Personality Disorder or Emotionally Unstable Personality Disorder
- Be able and willing to provide written informed consent to take part
- Have access to a personal computer, laptop, or smartphone and good quality internet for the purpose of completing questionnaires and any research interviews online
Exclusion criteria for all potential participants:
- Poor English literacy, so that the participant is unable to read the study materials.
- As a feasibility study, resources will not be sufficient to support non-English speaking or literate participants
Further information:
The carers’ group is an online group intervention for between 8 and 15 people, co-facilitated by a Mental Health professional and a carer with lived experience.
The group is made up of 12, weekly, 2-hour sessions, and covers 6 modules:
- The rights of carers, different presentations of emotional dysregulation
- Education related to the potential causes of emotional dysregulation
- Relationship mindfulness skills
- Communication environment creation skills
- Validation skills
- Collaborative problem-solving skills
If after screening, potential participants are eligible and consent to take part, they are randomly allocated to one of two groups:
- Participants in the ‘treatment’ group will receive the carers’ group intervention.
- Participants in the ‘treatment as usual’ group will continue to access any support services currently available.
For comparison, the same questionnaire data is gathered from both groups throughout the trial.
- At baseline, which is the beginning of the study
- At 14 weeks, which is following the intervention
- Follow up at 40 weeks, which is the evaluation end point
The questionnaires gather data on wellbeing, mental health and resource use. They can be completed online or on paper, with or without support from the research team.
Participants will receive a £20 voucher for every questionnaire they complete, which is a total of £60 in vouchers, if questionnaires are completed at all 3 stages.
In addition, some participants will be asked to take part in an interview to gain a deeper understanding about the process and experience of the trial and the intervention.
Contact information:
Alexandra Young (alexandra
Kieron Corrigan (kieron
This study closes on the 31st January 2025
Dementia
Research has revealed the prevalence of anxiety and depression in carers of people with dementia is higher than the general population. Care is usually offered by NHS psychological services, but this poses potential barriers to carers, such as mobility issues, lack of respite care access or long waiting lists.
Online treatments are a way to address this issue as they can be delivered remotely in the person’s own time. iACT4CARERS uses an online Acceptance and Commitment Therapy (ACT); a psychotherapy aiming to improve mood and quality of life. ACT does not aim to change thoughts and feelings, but reduce avoidance of them and enhance personally meaningful behaviour.
iACT4CARERS aims to understand the effectiveness of ACT in reducing symptoms of anxiety in carers.
To take part in this study, people must:
- Be over the age of 18 years old
- Be caring for a family member diagnosed with dementia
- Be experiencing anxieties or worries
- Have access to a smartphone, tablet or computer
- Have access to the internet
Further information:
The iACT4CARERS trial is a 12-week self-directed therapy. iACT4CARERS can be accessed from participant’s own home using a smartphone, tablet or computer.
Participants will be asked to complete eight, 40-60 minute, online sessions over this time and provide your reflections after each session. A trial therapist will support participants over this time, providing tailored written feedback after each session and two optional 30-minute phone calls.
Before enrolling in the study, participants will be asked to complete baseline questionnaires about themselves and their thoughts and feelings regarding their caregiving role. Participants will be asked to complete these again at 12-weeks and 24-weeks to assess the impact of ACT.
By completing the trial, participants will be entered into a prize draw to win one of 50, £20, gift vouchers.
Some participants will be invited to take part in an individual interview at the end of the study. This is optional.
This study closes on the 30 June 2025
Eating Disorders
EDGI is a project set up to explore risk factors in individuals who have experienced eating disorders, including anorexia nervosa, bulimia nervosa, binge-eating disorder or any other eating disorder at any time in their lives.
It aims to better understand the genetic and environmental links to eating disorders in order to improve treatments for current and future patients. EDGI is also part of the NIHR BioResource, which is a library of information about people’s health aiming to support research in both physical and mental health.
To take part in this study, people must:
- Be aged 16 and above
- Live in England
- Be currently experiencing or have experienced an eating disorder
The EGDI study process involves of four steps:
- Registering on the website edgiuk.org and reading the information sheet
- Providing consent using the online form (please put AWP as where you heard about the study)
- Completing a questionnaire
- Providing a saliva sample
AWP Research and Development contact:
This study will close on the 31 March 2028
Perinatal
The National Centre for Mental Health (NCMH) is heading an important research study called Maternal Wellbeing, Mental Health and Life Experiences.
This is an online survey that’s looking to understand more about how life experiences and COVID-19 have impacted on maternal wellbeing and mental health during the perinatal period.
We hope the findings will lead to new and improved ways of recognising and providing support in times of need.
The survey can be found here.
To take part in this study, people must:
- Be over 18-years-old
- Be pregnant or have given birth in the last 12 months
Individuals with or without a mental health diagnosis are welcome to complete the survey.
Participants will also be entered into a prize draw to win up to the value of £100 for their continued participation in the follow up maternal mental health surveys.
AWP Research and Development contacts:
Alexandra Young (alexandra
This study closes on the 31 March 2025
Physical health
Tobacco smoking remains a leading cause of ill health, early death, and causes health inequalities. Data from 2020 shows that hospital admissions due to smoking had risen 10% over 10 years ago. This costs the NHS £2.5 billion per year. The UK government set out an ambition to reduce the number of people that smoke to 5% or less by 2030.
Most NHS settings first offer smokers tobacco dependence treatment. This is an opt-in approach; where healthcare professionals can offer support to people that seek help to quit.
A different approach, where smokers are given treatment and support to quit smoking automatically, unless they choose to opt-out has been shown to double the number of people that quit.
This approach involves identifying smokers and providing support to quit through behavioural counselling and pharmacotherapy offered routinely through inpatient admissions, maternity services, and mental health settings.
The Tobacco Dependence Service (TDS) Evaluation aims to understand whether this service is effective. This includes what is working well, what could improve, and what makes a successful service.
To take part in staff interviews for this study, individuals must:
- Be a frontline healthcare professional, manager or supervisor involved in delivering or supporting the delivery of the NHS-funded TDS
- Work in acute, maternity, or mental health settings
To take part in service user interviews for this study, individuals must:
- Be aged 18 or over
- Be accessing acute settings where length of stay is greater than one day, maternity services or mental health inpatient services
- Have been in contact with a Tobacco Dependency Advisor
Further information for staff:
Individuals would take part in semi-structured interviews to explore the delivery of the TDS intervention, including the barriers and enablers to implementing the intervention.
The interviews can be face-to-face, over the phone or using a secure video conferencing platform. The interview would last for up to 1 hour.
Further information for service users:
Individuals would take part in semi-structured interviews about their understanding of and feelings towards the tobacco dependence intervention.
The interviews can be face-to-face, over the phone or using a secure video conferencing platform. The interview would last for up to 1 hour.
Further information for all who take part:
Individuals who take part in the study will be offered a £15 Amazon voucher as a thank you.
AWP Research and Development contacts:
Monalisa Bora-White (monalisa
Holly Spray (h
This study closes on 30 June 2025
Self-harm
Repeated self-harm is common, and is linked to other problems like lower quality of life and depression. The FReSH START RCT study team at the University of Leeds are running this study to see if adapted therapies are better at supporting people who self-harm, than therapies that are currently used in the NHS.
They have adapted three talking therapies that are currently used in the NHS. The study aims to see if these therapies improve quality of life and reduce self-damaging behaviours.
To take part in this study, people must:
- Have presented an Emergency Department (ED) for self-harm and have been assessed, as well as referred by the ED Team to the study
- Be registered with a GP in the catchment area of Avon and Wiltshire Mental Health Partnership NHS Trust for the duration of therapy
- Have mental capacity to provide fully informed consent
- Be aged 18 years or over
People cannot take part in this study if they:
- Are receiving, or been referred to, a specific psychological intervention that is similar to the trial intervention, or where a specific intervention is indicated for a related condition (e.g. anorexia nervosa) and would conflict with trial participation
- Have taken part in the FReSH START Feasibility Study
- Are assessed by a clinician as currently unsuitable for therapy. This may be due to individuals being in crisis, actively suicidal, past talking treatments leading to deterioration of mental state, diagnosis of schizophrenia, autism, or other severe mental illness that requires tailored talking therapies
- Lack capacity to comply with study requirements
- Have insufficient understanding of English to take part in talking therapy
- Have a known risk of violence
Further information:
People who decide to take part will be allocated randomly (like tossing a coin) to either the intervention or the standard care. If they are allocated to intervention, they will then be allocated randomly again to either adapted Cognitive Behaviour Therapy or adapted Psychodynamic Interpersonal Therapy.
Participants who are randomly allocated to the intervention will have up to 12 sessions of therapy with a trained therapist. The sessions will take around 45 minutes each and will be done over a 6 month period. For people who are allocated to standard care, they will receive the care that the Trust normally provides to people who self-harm. Sessions can take place online or in person.
During the study, monthly texts will be sent to participants to check in on how they are doing and whether they have self-harmed in the last month, these are secure and confidential texts.
All participants will be asked to complete questionnaires at the start of the study, then at 6 months and 12 months into the study about wellbeing. There will also be some shorter questionnaires to complete at 3 months and 9 months into the study.
Participants will get a £20 Amazon voucher for completing the questionnaires at 6 months from the start of the study, and a £40 Amazon voucher for completing the 12 month follow up questionnaires.
AWP Research and Development contacts:
This study will close on the 31 January 2025
Trauma
The National Centre for Mental Health (NCMH) is heading an important research study called National Centre for Mental Health Trauma Survey.
This is an online survey looking to understand more about trauma (experienced as a child and in adulthood) and its impact on mental health.
We hope the findings will help improve diagnosis, treatment and support for those who have experienced traumatic events.
To take part in this study people must:
- Be 18 years-old or over
- Have experienced a traumatic event, as a child or in adulthood
Individuals with or without a mental health diagnosis are welcome to complete the survey
Further information:
The online survey will take approximately 10-15 minutes and will ask you to:
- Provide your contact details (for example address, email address and phone number) and some personal information (for example date of birth, ethnic group and employment status).
- Answer some questions about your experiences of trauma (as a child and in adulthood) and your mental health.
The survey can be found here: https://ncmh-surveys.cardiff.ac.uk/redcap/surveys/?s=C48KA8AHP9JKLYDD&healthboard=avonandwiltshire
AWP Research and Development contact:
Jo Morris-Bone (jo
This study closes on the 31 March 2025
Participant in Research Experience Survey (PRES)
Click the button below to tell us about your experience of taking part in research.