Internet-delivered Cognitive Behavioural Therapy for Persons With Spinal Cord Injury

Sponsor
University of Regina (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT03963843
Collaborator
Lawson Health Research Institute (Other)
122
2
2
30.4
61
2

Study Details

Study Description

Brief Summary

In Canada the prevalence of spinal cord injury (SCI) is approximately 85,556, with incidence rates of traumatic and non-traumatic SCI at 1,785 and 2,286 cases per year, respectively. Common secondary health conditions experienced by individuals with SCI include psychological distress and pain. Appropriate management of these secondary conditions, through a multidisciplinary approach, is imperative as they have been shown to contribute to slower recovery, increased negative outcomes, and greater rates of rehospitalizations and health care utilization. However, resource limitations can restrict the ability of service providers to deliver these integrative biopsychosocial approaches in the community. Guided internet delivered cognitive behavioural therapy (ICBT) program offers an alternative approach for psychosocial service delivery in the community. The program provides online structured self-help modules based on the principles of cognitive behavioural therapy (CBT) in combination with guidance from a coach through weekly emails and telephone calls. ICBT was shown to have similar effects to face-to-face CBT. Results from the investigator's pilot pre-post study (ClinicalTrials.gov: NCT03457714), found significant effects of guided ICBT on primary outcome of depression (d=1.20, p=.02) post-intervention and gains were maintained at 3-month follow-up among persons with SCI. Significant improvements in secondary outcomes including pain interference, resilience, positive affect, self-efficacy, ability to participate, and grief were also found.These studies demonstrate that guided ICBT is a safe and effective alternative to face-to-face interventions and it may be beneficial for underserviced populations.

In the proposed trial, the investigators will examine the efficacy of the Guided ICBT Chronic Conditions Course for persons with SCI versus an online SCI Rehabilitation Education program. 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. As part of the battery of questionnaires administered after the completion of the program, clients will be asked to rate the program content, the overall service, and their satisfaction with the program.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Guided ICBT
  • Other: SCI rehabilitation mental health education
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
122 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Internet-delivered Cognitive Behavioural Therapy for Persons With Spinal Cord Injury: Randomized Controlled Trial
Actual Study Start Date :
Oct 18, 2019
Actual Primary Completion Date :
Nov 1, 2021
Anticipated Study Completion Date :
Apr 30, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: SCI internet delivered cognitive behavioural therapy

An 8-week internet- delivered cognitive behavioural therapy (ICBT) will be delivered to participants who have sustained a spinal cord injury. In addition to the online program, a health educator with experience delivering ICBT will provide support by email once a week. The health educator will spend approximately 15 minutes per week/per client.

Behavioral: Guided ICBT
An 8-week internet- delivered cognitive behavioural therapy (ICBT) will be delivered to participants who have sustained a spinal cord injury. In addition to the online program, a health educator with experience delivering ICBT will provide support by email once a week. The health educator will spend approximately 15 minutes per week/per client.

Active Comparator: SCI rehabilitation mental health education

Participants will receive information provided to SCI patients in usual care at specialized SCI rehabilitation units (the Spinal Cord Injury Rehabilitation Evidence (SCIRE) Community handouts available at: https://scireproject.com/community/handouts/). The lessons will include information on spinal cord injury rehabilitation: 1)spinal cord injury basics, 2)mental health after SCI, 3)pain after SCI, 4)understanding rehabilitation 5)summary of lessons through an online platform over 8 weeks. A health educator will check in with participants once a week to answer any content related questions. The health educator will spend approximately 15 minutes per week/per client.

Other: SCI rehabilitation mental health education
Participants will receive information provided to SCI patients in usual care at specialized SCI rehabilitation units (the Spinal Cord Injury Rehabilitation Evidence (SCIRE) Community handouts available at: https://scireproject.com/community/handouts/). The lessons will include information on spinal cord injury rehabilitation: 1)spinal cord injury basics, 2)mental health after SCI, 3)pain after SCI, 4)understanding rehabilitation 5)summary of lessons through an online platform over 8 weeks. A health educator will check in with participants once a week to answer any content related questions. The health educator will spend approximately 15 minutes per week/per client.

Outcome Measures

Primary Outcome Measures

  1. Change in depression [baseline, 8 weeks, 3 months, 6 months]

    Measured by Patient Health Questionnaire - 9 Item (PHQ-9), Higher scores indicate greater levels of depression. 0-4 No Depression, 5-9 Mild, 10-14 Moderate, 15-19 Moderately Severe, >19 Severe

  2. Change in anxiety [baseline, 8 weeks, 3 months, 6 months]

    Measured by Generalize Anxiety Disorder - 7 Item (GAD7), higher scores indicate greater level of anxiety. 0-4 Minimal, 5-9 Mild, 10-14 Moderate, 15-21 Severe

Secondary Outcome Measures

  1. Change in psychological distress [baseline, 8 weeks, 3 months, 6 months]

    Measured by Kessler 10-Item Scale, higher scores indicate greater level of distress, scores range 10-50

  2. Change in disability [baseline, 8 weeks, 3 months, 6 months]

    Measured by World Health Organization Disability Assessment Schedule - 12 Item, higher scores indicate greater level of disability. Scores range from 0-48.

  3. Change in quality of life symptoms: SCI-QoL-SF [baseline, 8 weeks, 3 months, 6 months]

    Spinal Cord Injury Quality of Life Short Form; SCI-QoL-SF, subscales of positive affect, resilience, self esteem higher scores indicate better function; subscale of grief/loss higher scores indicate severe symptoms.

  4. Change in pain: Brief Pain Inventory-Short Form [baseline, 8 weeks, 3 months, 6 months]

    Measured by Brief Pain Inventory-Short Form, the measure includes 4 items regarding pain intensity with scores ranging from 0-10 with higher scores indicating greater level of pain intensity; 7 items assess pain interference, scores ranging from 0-10 with higher scores indicating greater pain interference.

  5. Treatment credibility [baseline and 8 weeks]

    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.

  6. Treatment satisfaction: Internet-CBT Treatment Satisfaction Measure [baseline and 8 weeks]

    Measured by Internet-CBT Treatment Satisfaction Measure, each item is measured on a 0-4 scale, with higher scores indicating greater level of satisfaction.

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 spinal cord injury

  • 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 Lawson Health Research Institute London Ontario Canada N6C 2A1
2 Online Therapy Unit, University of Regina Regina Saskatchewan Canada S4S 0A2

Sponsors and Collaborators

  • University of Regina
  • Lawson Health Research Institute

Investigators

  • Principal Investigator: Heather Hadjistavropoulos, PhD, University of Regina
  • Principal Investigator: Swati Mehta, PhD, Lawson Health Research Institute

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University of Regina
ClinicalTrials.gov Identifier:
NCT03963843
Other Study ID Numbers:
  • 2019-020
First Posted:
May 28, 2019
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