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Reducing Stasis Outcomes for Depression in Group Behavioural Activation Therapy

Primary Purpose

Depression

Status
Completed
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Behavioural Activation Group (BAG) Psychotherapy
Sponsored by
University of Sheffield
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Depression focused on measuring Behavioural activation, Psychotherapy, group, Depression, Depressive disorder

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients who access the Sheffield Improving Access to Psychological Therapies (IAPT) service (United Kingdom) with depression as the primary presenting problem
  • Patients with co-morbid anxiety symptoms can be included as long as depression is the primary diagnosis
  • Are referred to and choose the Behavioural Activation Group (BAG) treatment option
  • Able to attend the BAG intervention
  • Aged 18 or over

Exclusion Criteria:

  • Primary diagnosis that is not depression
  • Patients who do not choose BAG as a treatment option
  • Aged under 18

Sites / Locations

  • Sheffield Health and Social Care NHS Foundation Trust - Improving Access to Psychological Therapies Service

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Enhanced Behavioural Activation Groups

Arm Description

Behavioural activation group (BAG) psychotherapy delivered with two embedded treatment augmentations; Implementation intentions Dose-response psychoeducation

Outcomes

Primary Outcome Measures

Change in Patient Health Questionnaire (PHQ-9) scores
Validated 9-item self-report measure of depressive symptoms

Secondary Outcome Measures

Patient attendance at treatment sessions
Number of therapy sessions patients attend in a course of treatment
Change in Valued Living Questionnaire (VLQ) score
Validated self-report measure of engagement in valued living
Change in Generalised Anxiety Disorder Assessment (GAD-7) score
Validated 7-item self-report measure of anxiety symptoms
Change in Work and Social Adjustment Scale (WSAS) score
Validated self-report measure of functional impairment as a result of mental health problems

Full Information

First Posted
November 11, 2016
Last Updated
May 1, 2018
Sponsor
University of Sheffield
Collaborators
Sheffield Health and Social Care NHS Foundation Trust, Howard Morton Trust
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1. Study Identification

Unique Protocol Identification Number
NCT02970279
Brief Title
Reducing Stasis Outcomes for Depression in Group Behavioural Activation Therapy
Official Title
Effect of Treatment Augmentations Embedded in Behavioural Activation Group Therapy on Reducing Drop-out and Stasis Rates in Depression
Study Type
Interventional

2. Study Status

Record Verification Date
May 2018
Overall Recruitment Status
Completed
Study Start Date
December 2016 (undefined)
Primary Completion Date
December 2017 (Actual)
Study Completion Date
December 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Sheffield
Collaborators
Sheffield Health and Social Care NHS Foundation Trust, Howard Morton Trust

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Depression is one of the most common mental health disorders and it is estimated up to 50% of patients do not respond to evidenced-based psychotherapy treatment, recording a 'stasis' outcome. However, there is limited research understanding this population, meaning a considerable number of people continue to suffer. The purpose of this study is to 1) identify depression stasis prevalence and predictors in an existing evidenced-based group treatment for depression, 2) run a clinical trial to test whether an embedded intervention based on theoretical and clinical practice evidence can help reduce patient depression stasis and drop-out rates and 3) understand what aspect of therapy produces change (or prevents change in stasis). The study will be based on behavioural activation (BA) therapy delivered in an eight-session group format in an Improving Access to Psychological Therapies (IAPT) service in the United Kingdom. BA is one of the most effective psychotherapies available for depression and focuses on helping patients to increase their engagement with valued activities to help break out of the cycle of depression. Firstly, an archived anonymised dataset of routine depression measures from patients who have previously received the existing group BA treatment will be analysed. Secondly, the group BA treatment delivered to patients in 2017 will be enhanced with two treatment augmentations. One augmentation will target stasis outcomes through the addition of specific 'if-then' planning (known as implementation intentions) when setting between-session homework and the other augmentation will target patient drop-out by informing patients about group BA effectiveness and therapy-dose evidence. The stasis outcomes and drop-out rates from the enhanced treatment in the trial will be compared with the archived outcomes to see if the intervention has had an effect and the role of engaging in valued living as a mechanism of change for depression symptoms will be examined. It is hypothesised that a) 50% of patients who have received the existing BA group treatment for depression will have a stasis outcome, b) there will be a significant reduction in depression stasis outcomes and drop-out rate following the enhanced BA group treatment delivered in the trial and c) engagement in valued living will have a mediating effect on outcome for responding patients following the enhanced BA group treatment but the effect will not be present for patients with a stasis outcome.
Detailed Description
A one-armed quasi-experimental trial will be used to test the effect of two embedded behavioural activation group (BAG) treatment augmentations on treatment outcomes and to identify a potential outcome mediator for patients with a stasis outcome. A non-randomised design enables data to be collected which reflects routine clinical practice and address stasis outcomes as they occur in real-world services. A matched pairs design will be implemented in the analysis to allow comparison of the enhanced BAG data with historical control data from archived outcomes of the existing treatment (i.e. the baseline data). Patients who access the Improving Access to Psychological Therapies (IAPT) service in Sheffield, United Kingdom with a primary presenting problem of depression and are referred to BAG will be approached to take part in the study. Patients will be asked to provide informed consent to agree for their weekly routine outcome scores from enhanced BAG to be used in the study. Enhanced BAG Augmentations The existing BAG treatment will be enhanced with embedded treatment augmentations. The augmentations will consist of two strands; 1) implementation intentions to directly target reducing stasis and 2) psychoeducation to target reducing drop-out. Implementation Intentions: The first augmentation will be a top-down theoretically informed 'implementation intentions' enhancement to target reducing the stasis outcome rate. Implementation intentions are specific plans about how, when and where goals will be acted upon, formed using an if-then format in order to effectively implement actions. Patients will be taught to use if-then planning (implementation intentions) to help them complete the between-session which is crucial to producing change in BA. Dose-Response Psychoeducation: The second augmentation will be a dose-response psychoeducation enhancement aimed at reducing the dropout rate. Patients will be given information based on practice-based evidence about the effectiveness of BAG and dose-response information (minimum number of sessions required to experience change). Treatment Integrity Treatment adherence to the protocol will be assessed using a BAG adherence checklist created for this trial. Adherence will be checked and compared using self-report and an expert rater; i) after each session the BAG facilitators will complete the session integrity measure to check self-report adherence and ii) the BAG facilitator lead will observe and rate one session from each course of BAG to provide an expert adherence check. Data Collection Data collection for the study will run for a year from January 2017 until December 2017 incorporating six BAG treatment groups. Data Analysis The data will be analysed using the intention-to-treat (ITT) principle. The final available measure will be used as the post score or if there is only one score available, it will be assumed there was no change. Patients who do not score above the clinical cut-off for depression (score of ≥10 on Patient Health Questionnaire [PHQ-9]) prior to commencing BAG will not be included in the analysis to avoid a floor effect when calculating stasis outcomes.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Depression
Keywords
Behavioural activation, Psychotherapy, group, Depression, Depressive disorder

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
34 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Enhanced Behavioural Activation Groups
Arm Type
Experimental
Arm Description
Behavioural activation group (BAG) psychotherapy delivered with two embedded treatment augmentations; Implementation intentions Dose-response psychoeducation
Intervention Type
Behavioral
Intervention Name(s)
Behavioural Activation Group (BAG) Psychotherapy
Intervention Description
Behavioural activation (BA) is a psychotherapy intervention based on behaviour theory and operant conditioning. It teaches patients to reduce avoidant depressive behaviours and in turn increase the positive reinforcement they receive from their environment for non-depressive behaviours through the use of activity scheduling and pleasant events. For the trial, BA will be delivered in a group format (BAG) and facilitated by two therapists. BAG treatment will consist of eight weekly sessions, lasting two hours and will follow a manualised treatment protocol. Each session will be based on a different topic relevant to the principles of BA and patients will be given between session work to complete to encourage increased participation in rewarding personally meaningful activities.
Primary Outcome Measure Information:
Title
Change in Patient Health Questionnaire (PHQ-9) scores
Description
Validated 9-item self-report measure of depressive symptoms
Time Frame
Week 1 (pre-treatment), at every weekly treatment session attended (for 8 weeks) and at week 8 (end of treatment)
Secondary Outcome Measure Information:
Title
Patient attendance at treatment sessions
Description
Number of therapy sessions patients attend in a course of treatment
Time Frame
Weeks 1-8 (every weekly treatment session - maximum of 8)
Title
Change in Valued Living Questionnaire (VLQ) score
Description
Validated self-report measure of engagement in valued living
Time Frame
Week 1 (pre-treatment), week 4 (at the 4th treatment session) and at week 8 (end of treatment)
Title
Change in Generalised Anxiety Disorder Assessment (GAD-7) score
Description
Validated 7-item self-report measure of anxiety symptoms
Time Frame
Week 1 (pre-treatment), at every weekly treatment session attended (for 8 weeks) and at week 8 (end of treatment)
Title
Change in Work and Social Adjustment Scale (WSAS) score
Description
Validated self-report measure of functional impairment as a result of mental health problems
Time Frame
Week 1 (pre-treatment), at every weekly treatment session attended (for 8 weeks) and at week 8 (end of treatment)
Other Pre-specified Outcome Measures:
Title
Behavioural activation group (BAG) therapy adherence
Description
BAG facilitators will complete an therapy adherence checklist (designed for this trial) after each session. An external rater will rate one session of each course of treatment to ensure adherence to the treatment protocol
Time Frame
Weeks 1-8 (Every treatment session)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients who access the Sheffield Improving Access to Psychological Therapies (IAPT) service (United Kingdom) with depression as the primary presenting problem Patients with co-morbid anxiety symptoms can be included as long as depression is the primary diagnosis Are referred to and choose the Behavioural Activation Group (BAG) treatment option Able to attend the BAG intervention Aged 18 or over Exclusion Criteria: Primary diagnosis that is not depression Patients who do not choose BAG as a treatment option Aged under 18
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Melanie K Simmonds-Buckley, BSc
Organizational Affiliation
University of Sheffield
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Stephen Kellett, DClinPsy
Organizational Affiliation
University of Sheffield & Sheffield Health and Social Care NHS Foundation Trust
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Glenn Waller, PhD
Organizational Affiliation
University of Sheffield
Official's Role
Principal Investigator
Facility Information:
Facility Name
Sheffield Health and Social Care NHS Foundation Trust - Improving Access to Psychological Therapies Service
City
Sheffield
State/Province
South Yorkshire
ZIP/Postal Code
S3 7ND
Country
United Kingdom

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
The data will be anonymised and analysed collectively so individual participant data will not be identifiable within any reports or publications.
Citations:
Citation
Gollwitzer, P. M. (1999). Implementation intentions: Strong effects of simple plans. American Psychologist, 54, 493-503.
Results Reference
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Reducing Stasis Outcomes for Depression in Group Behavioural Activation Therapy

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