- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT02902159
RCT of the Effectiveness of Big White Wall Compared to Other Online Support (REBOOT)
Randomised Controlled Trial of an Established Direct to Public Peer Support and E-therapy Programme (Big White Wall) Versus Information to Aid Self-management of Depression and Anxiety.
Studieöversikt
Status
Betingelser
Intervention / Behandling
Detaljerad beskrivning
Introduction
Unipolar depression and anxiety are respectively the second and seventh leading causes of years lived with disability in the world among all health problems according to the World Health Organisation. Self-support methods of management of depression and anxiety through a population approach such as online therapy and peer support is attractive for a number of reasons including: the scale of the problem and the ability of current services to cope; providing choice about the management of their symptoms; creating personal empowerment; developing supportive social networks; recurrence prevention.
The use of public health interventions for physical conditions such as cigarette smoking, weight loss and diabetes is increasingly utilised and effective in reaching the wider public.
Big White Wall
Big White Wall (BWW) is a well-established digital service (website and apps) 3 that offers:
- Online assessment of mental health problems and physical co-morbidities
- Moderated on-line peer support
- Guided support and live therapy
It is based on public health principles, emphasises a recovery model to improve well-being and is based theoretically on a social model of depression emphasising autonomy, hopefulness and support.
There are no waiting lists, eligibility criteria and opening hours (available 24/7).
It operates a community principle that each person is supported within cultures of respect, tolerance, mutual learning and safety, and procedures such as specially trained counsellors employed by BWW as "wall guides" try to ensure that this principle is maintained.
Patterns of use are often short-term over 3 to 6 weeks but people often utilise BWW at times of further need with a substantial proportion using it for longer periods on a more regular basis. Over that time people with depression and anxiety show clinically important improvement.
The case for online peer support interventions Peer support internet interventions such as BWW take less effort for service users than internet guided cognitive behaviour therapy (CBT) as it allows the user to choose when and how to access it rather than be committed to a pre-defined course of treatment. The overall effectiveness of BWW may be in keeping with the social model of depression and anxiety from which the website was conceived; that the onset of depression or anxiety may be precipitated by insufficient social support during a time of self-perceived threat to a person's well-being from a life event. Conversely, relief from depression or anxiety may be found through increased social support and improved life events and security.
BWW can therefore guide its users towards appropriate psycho-social support as and when they require it, whilst retaining autonomy through making their own decisions about how to use that support.
An important aspect of BWW's public health approach is to reach out to isolated people with poor quality social support and a perceived threat to their wellbeing. It aims to provide a population based service that doesn't require a personal subscription so that the most disadvantaged are able to benefit. Currently BWW has been purchased by the armed forces, some universities and 25% of Clinical Commissioning groups (CCGs) throughout England which provides free access to 98% of users.
However for a wider uptake by commissioners locally and nationally the service must be tested in a randomised controlled trial (RCT) to understand who, when and how BWW is utilised and its' clinical and cost effectiveness, compared to online information alone.
Trial Objectives To use the RE-AIM framework (Reach, Effectiveness, Adoption, Implementation including economics, Maintenance) to explore the efficacy and reach of an internet intervention (online peer support) compared to online information for people with depression and anxiety.
Use qualitative analysis to determine the engagement and experiences of the participants in the BWW arm of the study to understand the motivations for use, patterns and levels of engagement (e.g. active user versus 'lurker'), negative experiences and beliefs about efficacy and role in personal empowerment.
More specifically the trial objectives are:
- To determine the short-term clinical effectiveness of Big White Wall (BWW) versus the National Health Service (NHS) Choices Moodzone (MZ) website on well-being (primary outcome).
- To determine the number and representativeness of participants invited and eligible to receive BWW or the NHS Choices Moodzone website.
- To determine the number, percent and representativeness of NHS primary care practices and organisations, secondary care mental health, community and acute trust, third sector and social care organisations that referred people to either BWW or the NHS Choices Moodzone website
- To explore the implementation of the BWW programme including barriers and drivers to reach, effectiveness and adoption and an economic evaluation of its costs and cost effectiveness from personal, social and health care perspectives.
- To explore the maintenance of treatment effects on well-being, depressive symptoms, anxiety symptoms, quality of life and social function over 6 months in service users
- With Academic Helth Science Network (AHSN) East Midlands to record the take up by organisations and implementation (number, percent, representativeness in East Midlands) of BWW across the East Midlands after the trial has been completed
- Explore user engagement and experiences of BWW through qualitative interviews and text analysis
Expected duration in the trial is 6 months.
Implementation A managed network of practice will be established ideally with representation from the mental health leads from Nottingham City and Nottinghamshire CCGs and public health together with the User consultant and a GP Knowledge Broker as well as key members of National Institute of Health Research (NIHR) MindTech and the study team. This network will ensure that both the engagement strategy and the research project itself are optimised and that important learning on implementation is collected. The results of this RE-AIM study will provide a rich database of information to inform CCGs and Health and Wellbeing Boards on who BWW and other digital mental health services might reach Access to BWW across the East Midlands will depend on commissioning decisions at a public health and primary care level. At the end of the study we will work with AHSN East Midlands and Public Health England to present these findings to Directors of Public Health and mental health leads for each CCG or consortium of CCGs, Healthwatch representatives and mental health providers in the East Midlands together with a directory of alternative providers of similar services.
Studietyp
Inskrivning (Förväntat)
Fas
- Inte tillämpbar
Kontakter och platser
Studieorter
-
-
Nottinghamshire
-
Nottingham, Nottinghamshire, Storbritannien, NG7 2UH
- Rekrytering
- Nottingham University Hospitals NHS Trust
-
Nottingham, Nottinghamshire, Storbritannien, NG3 6AA
- Rekrytering
- Nottinghamshire Healthcare NHS foundation Trust.
-
-
Deltagandekriterier
Urvalskriterier
Åldrar som är berättigade till studier
Tar emot friska volontärer
Kön som är behöriga för studier
Beskrivning
Inclusion Criteria:
- Aged 16+
- Live in the County of Nottinghamshire, including Nottingham City
- Scores between10-20 on the Personal Health Questionnaire (PHQ9) and/or 10+ on Genral Anxiety Disorder Scale (GAD7)
- Access to internet through a pc or smartphone (Windows, iOS, Android)
- Able and willing to give informed consent
Exclusion Criteria:
- Scores 21 or more on the PHQ-9 (severe depression)
- And /Or Scores 2 or 3 on PHQ-9 item "thoughts that you would be better off dead or of hurting yourself in some way".
- Participant does not feel that they are sufficiently proficient in the use of the English Language (BWW and Moodzone are only available in English)
Studieplan
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Hälsovårdsforskning
- Tilldelning: Randomiserad
- Interventionsmodell: Parallellt uppdrag
- Maskning: Enda
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
---|---|
Experimentell: BWW
Free access to online peer support through BWW for 6 months
|
Free access to BWW online peer support and other services offered by them (except live therapy), for 6 months.
|
Experimentell: MZ
Access to NHS Moodzone Information Only
|
Directed to access to online information from NHS Moodzone
|
Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
---|---|---|
Warwick-Edinburgh Mental Well-being Scale - 14 Item
Tidsram: 6 weeks
|
Change on the 14-item Warwick-Edinburgh Mental Well-Being Scale (WEMWBS) from baseline to week 6
|
6 weeks
|
Sekundära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
---|---|---|
Warwick-Edinburgh Mental Well-being Scale - 14 Item
Tidsram: 12 and 26 weeks
|
Maintenance of effect
|
12 and 26 weeks
|
Generalised Anxiety Disorder 7 Item Scale (GAD-7)
Tidsram: 6, 12 & 26 weeks
|
Change in score on GAD7 at 6, 12 & 26 weeks
|
6, 12 & 26 weeks
|
Personal Health Questionnaire 9 Item (PHQ-9) 11
Tidsram: 6, 12 & 26 weeks
|
Change in score at 6, 12 & 26 weeks
|
6, 12 & 26 weeks
|
SF-12 v2 Health Survey 12
Tidsram: 6, 12 & 26 weeks
|
Change in score at 6, 12 & 26 weeks
|
6, 12 & 26 weeks
|
Work and Social Adjustment Scale 8 Item - Social Function 13
Tidsram: 6, 12 & 26 weeks
|
Change in score at 6, 12 & 26 weeks
|
6, 12 & 26 weeks
|
8-item social support measure14
Tidsram: 6, 12 & 26 weeks
|
Change in score at 6, 12 & 26 weeks
|
6, 12 & 26 weeks
|
12-item Brugha Inventory of Life Events15
Tidsram: 26 weeks
|
Change in score at 26 weeks
|
26 weeks
|
8-item Standardised Assessment of Personality-Abbreviated Scale (SAPAS
Tidsram: 26 weeks
|
Change in score at 6, 12 & 26 weeks
|
26 weeks
|
Andra resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
---|---|---|
Client Service Receipt Inventory (CSRI)
Tidsram: Baseline, 6, 12 & 26 weeks
|
Health Economics Measure
|
Baseline, 6, 12 & 26 weeks
|
Samarbetspartners och utredare
Sponsor
Utredare
- Huvudutredare: Richard Morriss, MD, CLAHRC-EM
Publikationer och användbara länkar
Allmänna publikationer
- Andrews G, Cuijpers P, Craske MG, McEvoy P, Titov N. Computer therapy for the anxiety and depressive disorders is effective, acceptable and practical health care: a meta-analysis. PLoS One. 2010 Oct 13;5(10):e13196. doi: 10.1371/journal.pone.0013196.
- Gulliver A, Griffiths KM, Christensen H. Perceived barriers and facilitators to mental health help-seeking in young people: a systematic review. BMC Psychiatry. 2010 Dec 30;10:113. doi: 10.1186/1471-244X-10-113.
- Mojtabai R, Olfson M, Sampson NA, Jin R, Druss B, Wang PS, Wells KB, Pincus HA, Kessler RC. Barriers to mental health treatment: results from the National Comorbidity Survey Replication. Psychol Med. 2011 Aug;41(8):1751-61. doi: 10.1017/S0033291710002291. Epub 2010 Dec 7.
- Crisp D, Griffiths K, Mackinnon A, Bennett K, Christensen H. An online intervention for reducing depressive symptoms: secondary benefits for self-esteem, empowerment and quality of life. Psychiatry Res. 2014 Apr 30;216(1):60-6. doi: 10.1016/j.psychres.2014.01.041. Epub 2014 Feb 3.
- Spiers N, Bebbington P, McManus S, Brugha TS, Jenkins R, Meltzer H. Age and birth cohort differences in the prevalence of common mental disorder in England: National Psychiatric Morbidity Surveys 1993-2007. Br J Psychiatry. 2011 Jun;198(6):479-84. doi: 10.1192/bjp.bp.110.084269.
- Happonen AP, Kaipainen K, Vaatanen A, Kinnunen ML, Myllymaki T, Lappalainen P, Tuomela H, Rusko H, Mattila E, Lappalainen R, Korhonen I. A concept to empower self-management of psychophysiological wellbeing: preliminary user study experiences. Annu Int Conf IEEE Eng Med Biol Soc. 2009;2009:312-5. doi: 10.1109/IEMBS.2009.5333549.
Användbara länkar
Studieavstämningsdatum
Studera stora datum
Studiestart
Primärt slutförande (Förväntat)
Avslutad studie (Förväntat)
Studieregistreringsdatum
Först inskickad
Först inskickad som uppfyllde QC-kriterierna
Första postat (Uppskatta)
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
Senast verifierad
Mer information
Termer relaterade till denna studie
Nyckelord
Ytterligare relevanta MeSH-villkor
Andra studie-ID-nummer
- CLAHRC-EM 16053
Plan för individuella deltagardata (IPD)
Planerar du att dela individuella deltagardata (IPD)?
Denna information hämtades direkt från webbplatsen clinicaltrials.gov utan några ändringar. Om du har några önskemål om att ändra, ta bort eller uppdatera dina studieuppgifter, vänligen kontakta register@clinicaltrials.gov. Så snart en ändring har implementerats på clinicaltrials.gov, kommer denna att uppdateras automatiskt även på vår webbplats .
Kliniska prövningar på Depression
-
ProgenaBiomeRekryteringDepression | Depression, postpartum | Depression, ångest | Depression Måttlig | Depression Svår | Klinisk depression | Depression i remission | Depression, Endogen | Depression KroniskFörenta staterna
-
Kintsugi Mindful Wellness, Inc.Sonar Strategies; Vituity PsychiatryRekryteringDepression | Depression Måttlig | Depression Svår | Depression MildFörenta staterna
-
University of California, San FranciscoRekryteringDepression Måttlig | Depression Mild | Depression, tonåringFörenta staterna
-
University GhentUniversiteit Antwerpen; Janssen-Cilag Ltd.Rekrytering
-
Washington University School of MedicineAvslutadBehandling Resistent depression | Senlivsdepression | Geriatrisk depression | Refraktär depression | Terapiresistent depressionFörenta staterna, Kanada
-
Baylor College of MedicineUniversity of TexasRekryteringDepression | Depression Måttlig | Depression Svår | Självmord och självskada | Depression i tonåren | Depression MildFörenta staterna
-
University of Cape TownNational Institute of Mental Health (NIMH)AvslutadPostpartum depression | Klinisk depression | Måttlig depressionSydafrika
-
Gerbera Therapeutics, Inc.Har inte rekryterat ännuPostpartum depression | Depression, postpartum | Postnatal depression | Post-partum depression | Post-Natal depressionFörenta staterna
-
Northern Illinois UniversityUniversity Autonoma de Santo DomingoAvslutadDepression Måttlig | Depression MildFörenta staterna, Dominikanska republiken
-
Charite University, Berlin, GermanyAvslutadBehandling Resistent depression | Depression, unipolär | Depression KroniskTyskland
Kliniska prövningar på BWW Online Peer Support
-
University College, LondonAvslutadDepression | Ångest | Ensamhet | Ångestsyndrom | Dåligt humörStorbritannien
-
Children's Mercy Hospital Kansas CityHar inte rekryterat ännu
-
The Hospital for Sick ChildrenAvslutad
-
University of Wisconsin, MadisonPatient-Centered Outcomes Research Institute; Community Place; Jewish Family... och andra samarbetspartnersAvslutadSjukhusinläggning | Akuten | HälsoprogramFörenta staterna
-
The Hospital for Sick ChildrenAvslutadJuvenil idiopatisk artritKanada
-
The Hospital for Sick ChildrenAvslutad
-
Duke UniversityNational Institute of Nursing Research (NINR)AvslutadFetma | Kardiovaskulär sjukdom | Cancer | Typ II diabetes | Kamratstöd och kroniska sjukdomarFörenta staterna
-
Children's National Research InstitutePatient-Centered Outcomes Research InstituteAvslutadFör tidig födelse av nyfödd | Sjuklighet hos nyfödda | Familj | Omogen nyfödd | Spädbarns nyfödda sjukdomFörenta staterna
-
University of RochesterAvslutadSubstansmissbruk | Infektiös endokardit | IV droganvändningFörenta staterna
-
Washington University School of MedicineAvslutad