CClinicalTrials.gg
Status unknownNCT02987608Updated Dec 9, 2016

A Feasibility Trial of Power Up

An interventional study of Power Up in Emotional Difficulties, sponsored by University College, London. Status unknown at 3 sites in United Kingdom. Open to participants aged 11 Years to 19 Years. Per ClinicalTrials.gov, last updated 2016-12-09.

Sponsored by University College, London · Not applicable, Interventional, and Supportive care

The sponsor has not verified this record recently (last verified Oct 2016), so the status shown — last known as Recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
120
Allocation
Non-randomized
Ages
11 Years to 19 Years
Sex
All
01

Study summary

There is an increasing demand for digital tools to empower young people with mental health difficulties (NHS England, 2015). Digital information, advice and mood tracking tools are increasingly being used to support child mental health. Evidence suggests that young people want to be active participants in their care and involved in decisions about their treatment. However, there is a lack of digital shared decision making tools available to support young people in Child and Adolescent Mental Health Services (CAMHS). This study aims to develop Power Up, a smartphone app to empower young people in CAMHS to make their voice heard and to participate more in decisions around their care.

The project will involve two phases:

  • Development Phase -Developing Power Up according to the views and ideas expressed by young people, their parents/ carers, and clinicians in Patient and Public Involvement (PPI) sessions. -Conducting interviews and focus groups with 10 young people in CAMHS, 10 parents/ carers and 10 clinicians to review the acceptability of the content and format of Power Up.
  • Feasibility testing Phase -Conducting a feasibility trial with 120 young people with emotional difficulties, aged 11-19 years, from three London CAMHS. 60 young people will receive treatment as usual and 60 will use Power Up alongside treatment as usual. Participant's ratings of empowerment, activation, and symptoms will be measured soon after their referral to the service. The same measures plus shared decision making questionnaires will be administered three months later.

The findings will inform the planning of a prospective cluster controlled trial. More broadly this trial will contribute an understanding of the feasibility and acceptability of developing and implementing a shared decision making app into CAMHS.

02

Conditions studied

  • Emotional Difficulties
03

In context

Lead sponsor

University College, London is the lead sponsor of 632 studies on the registry; 145 are open to participants now.

Of its 6 completed or terminated interventional studies of FDA-regulated products, 2 (33%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
11 Years to 19 Years
Sexes eligible
All
Accepts healthy volunteers
No

Eligibility criteria

Inclusion Criteria:

  • Recently been referred to CAMHS (pre - first appointment)
  • Presenting with emotional difficulties
  • Clinician will have confirmed that the young person does not have any vulnerability which would make taking part in the study inappropriate to their context
05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
120 participants (estimated)

Study arms

  • No intervention
    Control Phase (No Power Up)

    60 young people will receive CAMHS treatment as usual. Measures of empowerment, activation, and symptoms will be completed by participants soon after their referral to the service. The same measures plus shared decision making questionnaires will be administered three months later.

  • Experimental
    Intervention Phase (Power Up)

    60 young people use Power Up alongside CAMHS treatment as usual. Measures of empowerment, activation, and symptoms will be completed by participants soon after their referral to the service. The same measures plus shared decision making questionnaires and a Power Up feedback form will be administered three months later.

    Device: Power Up

Interventions

  • DevicePower Up

    Smartphone phone app

06

What researchers measure

Primary outcomes

  1. Shared Decision Making Questionnaire - 9 (SDM Q-9)

    This will be completed by young people at time two (three months into therapy). The SDM Q-9 is a nine item patient reported shared decision making questionnaire.

    Time frame: 3 months

  2. CollaboRATE

    This will be completed by young people at time two (three months into therapy). CollaboRATE is a three item patient reported shared decision making measure.

    Time frame: 3 months

  3. Experience of Service Questionnaire (ESQ)

    Four items from this questionnaire will be completed by young people at time two (three months into therapy) as a proxy measure of shared decision making. The ESQ is a self-completion questionnaire that assesses children and young people's views of services with respect to accessibility, humanity of care, organisation of care and environment.

    Time frame: 3 months

  4. Dyadic OPTION scale

    This will be completed by clinicians at time two (three months into therapy). The Dyadic OPTION scale is a 12- item instrument to measure the extent to which patients have been involved in shared decision making from the viewpoint of the clinician.

    Time frame: 3 months

Secondary outcomes

  1. Patient Activation Measure - Mental Health (PAM - MH)

    The PAM - MH will be completed by young people at time one (beginning of therapy) and time two (three months into therapy). The PAM - MH is a patient reported tool for measuring engagement in mental healthcare.

    Time frame: 3 months

  2. Strengths and Difficulties questionnaire (SDQ)

    The SDQ will be completed by young people at time one (beginning of therapy) and time two (three months into therapy). The SDQ is a self-report behavioural screening questionnaire for children and adolescents measuring symptoms and functioning.

    Time frame: 3 months

  3. Youth Efficacy / Empowerment Scale - Mental Health (YES - MH)

    The YES -MH will be completed by young people at time one (beginning of therapy) and time two (three months into therapy). The YES - MH assesses youth perceptions of efficacy with respect to managing their own mental health condition ('Self'), managing their own services and supports ('Service'), and using their experience and knowledge to help peers and improve service systems ('System').

    Time frame: 3 months

  4. Client Receipt of Services Inventory (CSRI) - Children's Version.

    The CSRI will be completed by parents at time one (beginning of therapy) and time two (three months into therapy). The CSRI provides information on service utilisation, as reported by the main carer of the child in the family.

    Time frame: 3 months

Other outcomes

  1. Did Not Attends (DNAs)

    Number of young person DNAs will be reported by the clinician.

    Time frame: 3 months

  2. Number of sessions attended

    The number of sessions attended by the young person will be reported by the clinician.

    Time frame: 3 months

  3. Type of therapy / intervention received

    The type of therapy / intervention received by the young person will be reported by the clinician.

    Time frame: 3 months

07

Study locations

3 of 3 sites recruiting
  • East London NHS Foundation Trust
    London, E1 5NF, United Kingdom
    Recruiting
  • North East London NHS Foundation Trust
    London, IG11 7LZ, United Kingdom
    Recruiting
  • The Tavistock and Portman NHS Foundation Trust
    London, NW3 5BA, United Kingdom
    Recruiting
08

References and documents

Publications

  • Chapman L, Edbrooke-Childs J, Martin K, Webber H, Craven MP, Hollis C, Deighton J, Law R, Fonagy P, Wolpert M. A Mobile Phone App to Support Young People in Making Shared Decisions in Therapy (Power Up): Study Protocol. JMIR Res Protoc. 2017 Oct 30;6(10):e206. doi: 10.2196/resprot.7694. PubMed 29084708 ↗

Individual participant data

Plan to share: No

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 9, 2016, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT02987608
Lead sponsor
University College, London
Collaborators
Anna Freud National Centre for Children and Families, MindTech Healthcare Technology Co-operative, Common Room Consulting Ltd, Create Marketing
Responsible party
Sponsor
First posted
Dec 9, 2016
Start date
Sep 2016
Primary completion
Aug 2017 (estimated)
Completion
Sep 2017 (estimated)
Last update
Dec 9, 2016

Study contacts

Louise N Chapman
Contact
louise.chapman@annafreud.org
020 7443 2205
Julian Edbrooke - Childs
Contact
julian.edbrooke-childs@annafreud.org
020 7443 2275
Miranda Wolpert, Professor
principal investigator · UCL & Anaa Freud National Centre for Children and Families

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Oct 2016. You cannot join it, but the record below documents what was studied.

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