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COMPASS Study: an Online Cognitive-behavioural Therapy (CBT) Program Treating Anxiety and Low Mood in Long-term Conditions During the COVID-19 Pandemic (COMPASS)

Primary Purpose

Treatment of Illness-related Distress in Physical LTCs

Status
Completed
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
COMPASS
Standard charity resources
Sponsored by
King's College London
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Treatment of Illness-related Distress in Physical LTCs

Eligibility Criteria

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

Inclusion Criteria:

  • Aged 18 or over
  • Have responded to sign posting advise from the LTC charity or responded to an advert placed on a LTC charity website expressing their interest in taking part in the study.
  • Speak English to a sufficiently high standard to allow them to interact with digital CBT programs.
  • Live in the UK and can provide contact details of their registered general practitioner
  • Have an email address to allow them to register with a digital CBT program and have a basic understanding of the internet.
  • Scores ≥3 on the shortened patient health questionnaire (PHQ-4) self-report measure of depression and anxiety in relation to their LTC and/or the COVID-19 pandemic.

Exclusion Criteria:

  • Evidence of alcohol and/or drug dependency, cognitive impairment, severe mental health disorders, including bipolar disorder or psychosis
  • Acute suicidal risk requiring a level of support that cannot be provided by therapists who are supporting patients remotely in their use of digital health interventions.
  • Receiving active psychological treatment. Active psychological treatment is defined as receiving treatment from a psychologist/counselor/therapist or engaging with other online psychological treatment interventions.

Sites / Locations

  • Health Psychology Section

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

COMPASS

Standard charity resources

Arm Description

Participants will be treated with an online CBT program that is specifically tailored to illness-related distress in the context of long-term conditions. Participants will also have access to the standard charity resources.

Participants will be directed to the standard resources provided by the charities involved in the study.

Outcomes

Primary Outcome Measures

Change in Patient Health Questionnaire Anxiety and Depression Scale (PHQ-ADS)
A composite measure of Generalised Anxiety Disorder questionnaire (GAD-7) and Patient Health Questionnaire (PHQ-9). Min score = 0, Max score = 48, with higher scores indicating higher levels of distress.

Secondary Outcome Measures

Change in Work and social adjustment scale (WSAS)
Social functioning. Min score = 0, Max score = 40 , with higher scores indicating greater functional impairment.
Change in EQ-5D-3L
Quality of life. Min score = 5, Max score = 15 , with higher scores more problems in the scale dimensions.
Change in Illness perception questionnaire - revised (IPQ-R), emotional subscale
IPQ-R tailored to COVID-19 to establish emotional responses regarding the COVID-19 pandemic. Min score = 0, Max score = 24 , with higher scores indicating higher emotional responses.
Change in Patient Health Questionnaire - (PHQ-9)
Depression. Min score = 0, Max score = 27, with higher scores indicating greater depression
Change in Generalised Anxiety Disorder scale (GAD-7)
Anxiety. Min score = 0, Max score = 21, with higher scores indicating greater anxiety
Change in bespoke illness-related distress measure (2 items)
Illness-related distress. Developed by research team. Min score = 0, Max score = 6, with higher scores indicating greater distress.
Change in Patient Activation Measure (PAM) short version (13 items).
Assess knowledge and confidence in illness self-management. Min score = 0, max score = 100, with higher scores indicating greater levels of knowledge and confidence.
The Patient Global Impression Scales of Severity (PGI-S)
Perceived symptom severity. 1 item. Min = 0, Max = 3, with higher scores indicating greater perceived symptom severity.
The Patient Global Impression Scales of Improvement (PGI-I)
Perceived symptom improvement. 1 item. Min = 0, Max = 6, with higher scores indicating greater perceived symptom deterioration.

Full Information

First Posted
August 12, 2020
Last Updated
March 29, 2022
Sponsor
King's College London
Collaborators
National Multiple Sclerosis Society, Psoriasis Association, Crohn's & Colitis UK, Kidney Care UK, Shift.ms
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1. Study Identification

Unique Protocol Identification Number
NCT04535778
Brief Title
COMPASS Study: an Online Cognitive-behavioural Therapy (CBT) Program Treating Anxiety and Low Mood in Long-term Conditions During the COVID-19 Pandemic
Acronym
COMPASS
Official Title
Pilot RCT for COMPASS: an Online CBT Program Treating Anxiety and Low Mood in Long-term Conditions During the COVID-19 Pandemic.
Study Type
Interventional

2. Study Status

Record Verification Date
February 2021
Overall Recruitment Status
Completed
Study Start Date
November 16, 2020 (Actual)
Primary Completion Date
July 1, 2021 (Actual)
Study Completion Date
January 1, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
King's College London
Collaborators
National Multiple Sclerosis Society, Psoriasis Association, Crohn's & Colitis UK, Kidney Care UK, Shift.ms

4. Oversight

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

5. Study Description

Brief Summary
This study is a single-centre, interventional randomised controlled trial. Participants will be individually randomised to receive either COMPASS online CBT + "usual care" (standard LTC charity support), or usual care only. Randomisation will be stratified by recruiting charity site to ensure a balance of participants with different LTCs across the intervention and control arm. Randomisation will occur using a 1:1 allocation ratio managed by RECAP software. Participants randomised to COMPASS will receive access to the online program. It consists of 11 online modules which target challenges associated with living with LTC(s) and includes, amongst other things, psycho-education, patient examples, interactive tasks and goal setting. Participants are linked to a therapist; 'guide', who will provide 6 x 30 minute support sessions delivered fortnightly in the format preferred by the client (phone and/or in-site message). Participants allocated to the usual care control arm will receive the usual care that is available to them via their charity. All charities include a helpline which can be accessed via telephone or email. The helplines at all charities offer one-off emotional and/or informational support provided by people trained in active listening and/or counselling skills. Additional support avenues that can be accessed may include online support groups, local community support groups and informational resources.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Treatment of Illness-related Distress in Physical LTCs

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
194 (Actual)

8. Arms, Groups, and Interventions

Arm Title
COMPASS
Arm Type
Experimental
Arm Description
Participants will be treated with an online CBT program that is specifically tailored to illness-related distress in the context of long-term conditions. Participants will also have access to the standard charity resources.
Arm Title
Standard charity resources
Arm Type
Active Comparator
Arm Description
Participants will be directed to the standard resources provided by the charities involved in the study.
Intervention Type
Behavioral
Intervention Name(s)
COMPASS
Intervention Description
An 11 module, therapist-supported online CBT program.
Intervention Type
Behavioral
Intervention Name(s)
Standard charity resources
Intervention Description
Resources provided by the charities involved, including supportive listening, online support groups, information resources and local community support groups.
Primary Outcome Measure Information:
Title
Change in Patient Health Questionnaire Anxiety and Depression Scale (PHQ-ADS)
Description
A composite measure of Generalised Anxiety Disorder questionnaire (GAD-7) and Patient Health Questionnaire (PHQ-9). Min score = 0, Max score = 48, with higher scores indicating higher levels of distress.
Time Frame
At baseline, 6 weeks (mid-therapy) and 12 weeks (end of therapy)
Secondary Outcome Measure Information:
Title
Change in Work and social adjustment scale (WSAS)
Description
Social functioning. Min score = 0, Max score = 40 , with higher scores indicating greater functional impairment.
Time Frame
At baseline, 6 weeks (mid-therapy) and 12 weeks (end of therapy)
Title
Change in EQ-5D-3L
Description
Quality of life. Min score = 5, Max score = 15 , with higher scores more problems in the scale dimensions.
Time Frame
At baseline, 6 weeks (mid-therapy) and 12 weeks (end of therapy)
Title
Change in Illness perception questionnaire - revised (IPQ-R), emotional subscale
Description
IPQ-R tailored to COVID-19 to establish emotional responses regarding the COVID-19 pandemic. Min score = 0, Max score = 24 , with higher scores indicating higher emotional responses.
Time Frame
At baseline, 6 weeks (mid-therapy) and 12 weeks (end of therapy)
Title
Change in Patient Health Questionnaire - (PHQ-9)
Description
Depression. Min score = 0, Max score = 27, with higher scores indicating greater depression
Time Frame
At baseline, 6 weeks (mid-therapy) and 12 weeks (end of therapy)
Title
Change in Generalised Anxiety Disorder scale (GAD-7)
Description
Anxiety. Min score = 0, Max score = 21, with higher scores indicating greater anxiety
Time Frame
At baseline, 6 weeks (mid-therapy) and 12 weeks (end of therapy)
Title
Change in bespoke illness-related distress measure (2 items)
Description
Illness-related distress. Developed by research team. Min score = 0, Max score = 6, with higher scores indicating greater distress.
Time Frame
At baseline, 6 weeks (mid-therapy) and 12 weeks (end of therapy)
Title
Change in Patient Activation Measure (PAM) short version (13 items).
Description
Assess knowledge and confidence in illness self-management. Min score = 0, max score = 100, with higher scores indicating greater levels of knowledge and confidence.
Time Frame
At baseline, 6 weeks (mid-therapy) and 12 weeks (end of therapy)
Title
The Patient Global Impression Scales of Severity (PGI-S)
Description
Perceived symptom severity. 1 item. Min = 0, Max = 3, with higher scores indicating greater perceived symptom severity.
Time Frame
At baseline, 6 weeks (mid-therapy) and 12 weeks (end of therapy)
Title
The Patient Global Impression Scales of Improvement (PGI-I)
Description
Perceived symptom improvement. 1 item. Min = 0, Max = 6, with higher scores indicating greater perceived symptom deterioration.
Time Frame
6 weeks (mid-therapy) and 12 weeks (end of therapy)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Aged 18 or over Have responded to sign posting advise from the LTC charity or responded to an advert placed on a LTC charity website expressing their interest in taking part in the study. Speak English to a sufficiently high standard to allow them to interact with digital CBT programs. Live in the UK and can provide contact details of their registered general practitioner Have an email address to allow them to register with a digital CBT program and have a basic understanding of the internet. Scores ≥3 on the shortened patient health questionnaire (PHQ-4) self-report measure of depression and anxiety in relation to their LTC and/or the COVID-19 pandemic. Exclusion Criteria: Evidence of alcohol and/or drug dependency, cognitive impairment, severe mental health disorders, including bipolar disorder or psychosis Acute suicidal risk requiring a level of support that cannot be provided by therapists who are supporting patients remotely in their use of digital health interventions. Receiving active psychological treatment. Active psychological treatment is defined as receiving treatment from a psychologist/counselor/therapist or engaging with other online psychological treatment interventions.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Rona Moss-Morris
Organizational Affiliation
King's College London
Official's Role
Principal Investigator
Facility Information:
Facility Name
Health Psychology Section
City
London
ZIP/Postal Code
SE1 9RT
Country
United Kingdom

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
The data that support the findings of this study will be available on request from the corresponding author. The data will not be available publicly due to privacy or ethical restrictions.
IPD Sharing Access Criteria
The data will only be available on request.
Citations:
PubMed Identifier
34697123
Citation
Hulme K, Hudson JL, Picariello F, Seaton N, Norton S, Wroe A, Moss-Morris R. Clinical efficacy of COMPASS, a digital cognitive-behavioural therapy programme for treating anxiety and depression in patients with long-term physical health conditions: a protocol for randomised controlled trial. BMJ Open. 2021 Oct 25;11(10):e053971. doi: 10.1136/bmjopen-2021-053971.
Results Reference
derived

Learn more about this trial

COMPASS Study: an Online Cognitive-behavioural Therapy (CBT) Program Treating Anxiety and Low Mood in Long-term Conditions During the COVID-19 Pandemic

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