Internet-delivered Cognitive Behaviour Therapy for Chronic Conditions: Comparing Low Intensity Delivery Models

Sponsor
University of Regina (Other)
Overall Status
Completed
CT.gov ID
NCT03500237
Collaborator
(none)
188
1
2
40.3
4.7

Study Details

Study Description

Brief Summary

Chronic health conditions (e.g., heart disease, cancer, diabetes) represent any physical condition that persist for 3 months or more that requires ongoing management. Chronic health conditions are very common, and increase in prevalence with age. Internet-delivered Cognitive Behaviour Therapy (ICBT) is a promising approach for overcoming these barriers, and improving access to mental health care. In ICBT, clients receive content from traditional face-to-face CBT over the Internet, while receiving support and assistance from a guide through secure e-mail. The Chronic Conditions Course is an 8-week, 5 lesson ICBT program that consists of education and relapse prevention as well as cognitive, behavioural, and physical strategies for managing chronic conditions. This intervention has traditionally been delivered either with no support or with weekly brief (15 minute) individual therapist guidance via email and phone. However, in order to provide a faster response to clients using an on the demand (responding as quickly as possible and for sure within one business day team based approach (e.g., first available therapist responds) may be beneficial.

The proposed trial will examine the Chronic Conditions Course delivered by a team at the Online Therapy Unit based at the University of Regina versus a self-directed program. In the team based approach, participants will be able to contact the Online Therapy Unit if they have any questions regarding the content of the Chronic Conditions Course during the 8 week program. Participants in this group will receive a response from one of the members of the team within one business day. In the self-directed group, clients will receive automatic messages from the Online Therapy Unit that encourage participation during the 8 week program but otherwise will work on the course on their own. All participants will complete questionnaires prior to the start of the program, before each lesson of the program, once they have completed the program, and 3 months after completing the program. The primary outcome measures include anxiety and depression. Secondary outcomes include fatigue, pain, self-efficacy, disability, overall quality of life, and life satisfaction.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Team-Guided ICBT
  • Behavioral: Self-Guided ICBT
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
188 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Effectiveness of Internet-delivered Cognitive Behaviour Therapy for Chronic Conditions: Comparing Low Intensity Delivery Models
Actual Study Start Date :
Apr 16, 2018
Actual Primary Completion Date :
Aug 24, 2021
Actual Study Completion Date :
Aug 24, 2021

Arms and Interventions

Arm Intervention/Treatment
Experimental: Team-Guided ICBT

An 8-week transdiagnostic internet-delivered cognitive behavioural therapy (ICBT) for persons with chronic conditions course will be delivered to participants. In addition to the online program, a guide from the Online Therapy Unit team will provide support within one business day of the client's email. The team of guides consist of registered social workers, psychologists or supervised graduate students, with experience delivering ICBT. Amount of contact will be personalized to participants' needs.

Behavioral: Team-Guided ICBT
An 8-week transdiagnostic internet-delivered cognitive behavioural therapy (ICBT) for persons with chronic conditions course will be delivered to participants. In addition to the online program, a guide from the Online Therapy Unit team will respond within one business day of the client's email. The team of guides consist of registered social workers, psychologists or supervised graduate students, with experience delivering ICBT. Amount of contact will be personalized to participants' needs.

Active Comparator: Self-Guided ICBT

An 8-week transdiagnostic internet-delivered cognitive behavioural therapy (ICBT) for persons with chronic conditions course will be delivered to participants. Participants are able to contact the Online Therapy Unit regarding any technical issues with logging onto the site. However, no psychological intervention will be provided. A team member from the Unit will contact the participant only if there is a significant clinical issue requiring attention (e.g., sudden increase in symptoms).

Behavioral: Self-Guided ICBT
An 8-week transdiagnostic internet-delivered cognitive behavioural therapy (ICBT) for persons with chronic conditions course will be delivered to participants. Participants are able to contact the Online Therapy Unit regarding any technical issues with logging onto the site. However, no psychoeducational support will be provided. A team member from the Unit will contact the participant only if there is a significant clinical issue requiring attention (e.g., sudden increase in symptoms).

Outcome Measures

Primary Outcome Measures

  1. Change in depression [baseline, 8 weeks, 3 months]

    Measured by Patient Health Questionnaire - 9 Item (PHQ-9)

  2. Change in anxiety [baseline, 8 weeks, 3 months]

    Measured by Generalize Anxiety Disorder - 7 Item (GAD7)

Secondary Outcome Measures

  1. Change in psychological distress [baseline, 8 weeks, 3 months]

    Measured by Kessler 10-Item Scale

  2. Change in disability [baseline, 8 weeks, 3 months]

    Measured by World Health Organization Disability Assessment Schedule - 12 Item

  3. Change in quality of life symptoms [baseline, 8 weeks, 3 months]

    Measured by 5-level EuroQol-5D version (EQ-5D-5L), items are added for a score ranging from 5-25 with total score indicating: 5-14 Mild problem, 15-24 Moderate, 25 Worst Health State

  4. Change in pain [baseline, 8 weeks, 3 months]

    Measured by Brief Pain Inventory-Short Form

  5. Change in fatigue [baseline, 8 weeks, 3 months]

    Measured by Fatigue Symptom Inventory

  6. Change in life satisfaction [baseline, 8 weeks, 3 months]

    Measured by Satisfaction with Life Scale (SwLS), items are added together to get a score ranging from 5-35; Higher scores are indicative of greater life satisfaction

  7. Change in self-efficacy [baseline, 8 weeks, 3 months]

    Measured by Self-Efficacy for Managing Chronic Disease 6-item Scale

  8. Change in treatment costs [baseline, 3 months]

    Measured by Treatment Inventory of Costs in Psychiatric Patients (TIC-P) Adapted for Canada

  9. Treatment credibility [baseline]

    Measured by Treatment Credibility Questionnaire (TCQ) which contains 4 items. The first three items range from 0-9 with higher scores indicating better outcome, and the fourth item ranges from 0-100%, with higher scores indicating greater improvement in functioning.

  10. Treatment satisfaction [8 weeks]

    Measured by Internet-CBT Treatment Satisfaction Measure

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • 18 years of age or older

  • residing in Canada

  • endorsing symptoms of anxiety or depression

  • diagnosed with a chronic medical health condition

  • chronic condition does not impact ability to complete treatment (ex. cognitive impairment)

  • able to access a computer and internet service

  • willing to provide a physician as emergency contact

Exclusion Criteria:
  • high suicide risk

  • suicide attempt or hospitalization in the last year

  • primary problems with psychosis, alcohol or drug problems, mania

  • currently receiving active psychological treatment for anxiety or depression

  • not present in country during treatment

  • concerns about online therapy

Contacts and Locations

Locations

Site City State Country Postal Code
1 Online Therapy Unit, University of Regina Regina Saskatchewan Canada S4S 0A2

Sponsors and Collaborators

  • University of Regina

Investigators

  • Principal Investigator: Heather Hadjistavropoulos, PhD, University of Regina

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University of Regina
ClinicalTrials.gov Identifier:
NCT03500237
Other Study ID Numbers:
  • 2018-045
First Posted:
Apr 18, 2018
Last Update Posted:
Dec 16, 2021
Last Verified:
Dec 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by University of Regina
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 16, 2021