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Evaluating the Effects of a Self-help Mobile Phone Application on Worry and Overthinking in Young Adults Aged Between 16 and 24.

Primary Purpose

Rumination, Worry, Repetitive Negative Thinking

Status
Completed
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
digital CBT self-help including specific intervention elements to target worry and rumination.
Sponsored by
University of Exeter
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Rumination

Eligibility Criteria

16 Years - 24 Years (Child, Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • aged 16 to 24 years old (inclusive)
  • currently based in the UK
  • possess a basic literacy in English
  • able to provide informed consent
  • reporting elevated levels of worry and rumination, defined here as scoring above the 50th percentile (i.e., top-half of scale) on either the RSS (>34) or the PSWQ (>41)
  • have regular access to a smartphone (android or iOS).

Exclusion Criteria:

  • reporting highly elevated symptoms of depression indicating more specialist treatment is required (PHQ-9 > 20)
  • self-report of active suicidality
  • self-report currently receiving psychological therapy, counseling, or psychiatric medication, including antidepressants, for a current mental health condition

Sites / Locations

  • University of Exeter

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

waiting list control group

treatment group

Arm Description

Participants randomly allocated to this arm will be offered self-help components within a mobile phone app to target worry and rumination after a 6-week wait.

Participants randomly allocated to this arm will be offered self-help components within a mobile phone app to target worry and rumination immediately.

Outcomes

Primary Outcome Measures

Change in rumination using the Ruminative Response Scale (RRS)
A well established 22-item measure of pathological rumination which predicts subsequent depression.

Secondary Outcome Measures

Change in worry using the Penn State Worry Questionnaire (PSWQ)
a well-validated 16-item measure of trait tendency towards worry
Change in symptoms for depression using the Patient Health Questionnaire-9 (PHQ-9)
a well-validated measure of depression and depressive symptoms
Change in wellbeing using the Warwick-Edinburgh Mental Well Being Scale (WEMWBS)
a leading validated self-reported index of well-being with excellent psychometric properties comprising 14 items
Change in symptoms for anxiety using the Generalized Anxiety Disorder-7 (GAD-7)
A well validated measure of anxiety and anxiety symptoms

Full Information

First Posted
June 22, 2021
Last Updated
January 30, 2022
Sponsor
University of Exeter
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1. Study Identification

Unique Protocol Identification Number
NCT04950257
Brief Title
Evaluating the Effects of a Self-help Mobile Phone Application on Worry and Overthinking in Young Adults Aged Between 16 and 24.
Official Title
Evaluating the Effects of a Self-help Mobile Phone Application on Worry and Rumination Experienced by Young Adults: a Preventative Intervention for Depression and Anxiety
Study Type
Interventional

2. Study Status

Record Verification Date
January 2022
Overall Recruitment Status
Completed
Study Start Date
May 14, 2021 (Actual)
Primary Completion Date
December 13, 2021 (Actual)
Study Completion Date
January 30, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Exeter

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This project seeks to understand if a new self-help mobile phone application (called MyMoodCoach) is effective at reducing worry and overthinking, prominent risk factors that predict reduced well-being and poor mental health. As a primary outcome, the investigators are predicting that people who use the app will report more significant reductions on measures of overthinking than those who do not. The investigators also predict that people who use the app will report more significant reductions in measures of worry as well as reported symptoms of depression and anxiety. Further, it is predicted that people who use the app will report a significantly higher increase in their well-being compared to those who do not.
Detailed Description
The Emotional Competence for Well-Being in Young Adults study has developed an emotional competence app to be examined via cohort multiple randomised controlled trial (cmRCT) in a longitudinal prospective cohort. This off-shoot study adapts the app to focus on targeting worry and overthinking (also known as rumination), which are prominent risk factors for poor mental health. Within this study, 16-24-year-olds in the UK, who report elevated worry and rumination on standardised questionnaires are randomised to either receive the mobile phone app immediately or to receive the app after a wait of 6 weeks. In total, the study will aim to recruit 204 participants across the UK. Assessments take place at baseline (pre-randomisation), 6 and 12 weeks post-randomisation. Primary endpoint for the study is the change in levels of rumination assessed at 6 weeks after randomisation. Worry, depressive symptoms, anxiety symptoms and well-being are secondary outcomes. Compliance, adverse events, and potentially mediating variables will be carefully monitored. This trial aims to provide a better understanding of the benefits of tackling rumination and worry via an intervention delivered via mobile phone app with respect to promoting well-being and preventing poor mental health in young people. This prevention mechanism trial will establish whether targeting worry and rumination directly via an app provides a feasible approach to prevent depression and anxiety, with scope to become a widescale public health strategy for preventing poor mental health and promoting well-being in young people.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Rumination, Worry, Repetitive Negative Thinking

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
The trial design is of a superiority two-arm parallel-group single-blind randomised controlled trial comparing usual practice plus up to 6 weeks of using the repetitive negative thinking-targeting digital self-help app versus usual practice and waiting list control. The primary hypothesis is that the rumination-targeting digital self-help app will reduce rumination and worry significantly more than waiting list control at 6 weeks follow-up.
Masking
Outcomes Assessor
Masking Description
The analysis team members will be blind to the randomisation process and group allocation of participants
Allocation
Randomized
Enrollment
236 (Actual)

8. Arms, Groups, and Interventions

Arm Title
waiting list control group
Arm Type
Active Comparator
Arm Description
Participants randomly allocated to this arm will be offered self-help components within a mobile phone app to target worry and rumination after a 6-week wait.
Arm Title
treatment group
Arm Type
Experimental
Arm Description
Participants randomly allocated to this arm will be offered self-help components within a mobile phone app to target worry and rumination immediately.
Intervention Type
Device
Intervention Name(s)
digital CBT self-help including specific intervention elements to target worry and rumination.
Other Intervention Name(s)
MyMoodCoach
Intervention Description
The self-help app includes self-monitoring, psychoeducation and active self-help exercises. The self-monitoring includes daily mood ratings and an ecological momentary assessment option (MoodTracker) for more detailed analysis of mood, worry, activity and situational context. The digital self-help provides psychoeducation, tips, advice, exercises and training for each individual focused on reducing worry and rumination, using strategies from the proven rumination-focused CBT intervention. The app includes text, pictures, audio-recordings, animations, audio-exercises to practice (e.g., self-compassion, relaxation, concreteness exercises), and questionnaires with tailored feedback. The app is designed for iOS and Android use.
Primary Outcome Measure Information:
Title
Change in rumination using the Ruminative Response Scale (RRS)
Description
A well established 22-item measure of pathological rumination which predicts subsequent depression.
Time Frame
Change from baseline at 6 weeks
Secondary Outcome Measure Information:
Title
Change in worry using the Penn State Worry Questionnaire (PSWQ)
Description
a well-validated 16-item measure of trait tendency towards worry
Time Frame
Change from baseline at 6 weeks
Title
Change in symptoms for depression using the Patient Health Questionnaire-9 (PHQ-9)
Description
a well-validated measure of depression and depressive symptoms
Time Frame
Change from baseline at 6 weeks
Title
Change in wellbeing using the Warwick-Edinburgh Mental Well Being Scale (WEMWBS)
Description
a leading validated self-reported index of well-being with excellent psychometric properties comprising 14 items
Time Frame
Change from baseline at 6 weeks
Title
Change in symptoms for anxiety using the Generalized Anxiety Disorder-7 (GAD-7)
Description
A well validated measure of anxiety and anxiety symptoms
Time Frame
Change from baseline at 6 weeks
Other Pre-specified Outcome Measures:
Title
Change in worry using the Penn State Worry Questionnaire (PSWQ)
Description
a well-validated 16-item measure of trait tendency towards worry
Time Frame
Change from 6 weeks post randomisation at 12 weeks post randomisation
Title
Change in rumination using the Ruminative Response Scale (RRS)
Description
A well established 22-item measure of pathological rumination which predicts subsequent depression.
Time Frame
Change from 6 weeks post randomisation at 12 weeks post randomisation
Title
Change in symptoms for depression using the Patient Health Questionnaire-9 (PHQ-9)
Description
a well-validated measure of depression and depressive symptoms
Time Frame
Change from 6 weeks post randomisation at 12 weeks post randomisation
Title
Change in wellbeing using the Warwick-Edinburgh Mental Well Being Scale (WEMWBS)
Description
a leading validated self-reported index of well-being with excellent psychometric properties comprising 14 items
Time Frame
Change from 6 weeks post randomisation at 12 weeks post randomisation
Title
Change in symptoms for anxiety using the Generalized Anxiety Disorder-7 (GAD-7)
Description
A well validated measure of anxiety and anxiety symptoms
Time Frame
Change from 6 weeks post randomisation at 12 weeks post randomisation

10. Eligibility

Sex
All
Minimum Age & Unit of Time
16 Years
Maximum Age & Unit of Time
24 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: aged 16 to 24 years old (inclusive) currently based in the UK possess a basic literacy in English able to provide informed consent reporting elevated levels of worry and rumination, defined here as scoring above the 50th percentile (i.e., top-half of scale) on either the RSS (>34) or the PSWQ (>41) have regular access to a smartphone (android or iOS). Exclusion Criteria: reporting highly elevated symptoms of depression indicating more specialist treatment is required (PHQ-9 > 20) self-report of active suicidality self-report currently receiving psychological therapy, counseling, or psychiatric medication, including antidepressants, for a current mental health condition
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ed R Watkins, Professor
Organizational Affiliation
Exeter University
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Dan J Edge, MRes
Organizational Affiliation
Exeter University
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Exeter
City
Exeter
State/Province
Devon
ZIP/Postal Code
EX2 5DY
Country
United Kingdom

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
De-identified individual participant and clinical and economic data reported in publications will be made available through the University of Exeter's Institutional Repository - Open Research Exeter (see https://ore.exeter.ac.uk).
IPD Sharing Time Frame
The study protocol and informed consent form will be uploaded with this registration. The SAP is included in the study protocol. Data Access: Post-analysis, the final anonymised dataset will preferentially be stored in Open Research Exeter (ORE), the University of Exeter's open access repository. The data will be available from 24 months after trial completion (end of December 2021).
IPD Sharing Access Criteria
Access to these data is permitted but controlled through requests made via the repository to a review panel from the trial team, led by the chief investigator, which will assess requests on scientific merit and commercial sensitivity. Although use is permitted, this will be on the basis that the source of the data is acknowledged (including the funder) and it includes reference to the data set 'handle', and a data access agreement is signed, subject to approval by funder.
Citations:
PubMed Identifier
34674669
Citation
Edge D, Newbold A, Ehring T, Rosenkranz T, Frost M, Watkins ER. Reducing worry and rumination in young adults via a mobile phone app: study protocol of the ECoWeB (Emotional Competence for Well-Being in Young Adults) randomised controlled trial focused on repetitive negative thinking. BMC Psychiatry. 2021 Oct 21;21(1):519. doi: 10.1186/s12888-021-03536-0.
Results Reference
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Evaluating the Effects of a Self-help Mobile Phone Application on Worry and Overthinking in Young Adults Aged Between 16 and 24.

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