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Guided Internet Delivered Cognitive-Behaviour Therapy for Persons With Spinal Cord Injury: A Feasibility Trial

Guided Internet Delivered Cognitive-Behaviour Therapy for Persons With Spinal Cord Injury: A Feasibility Trial

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03457714
Enrollment
20
Registered
2018-03-07
Start date
2017-09-07
Completion date
2018-12-31
Last updated
2019-04-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anxiety, Depression, Spinal Cord Injuries

Keywords

spinal cord injuries, anxiety, depression, internet-delivered cognitive behaviour therapy, pilot study

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. In Canada over 37% of individuals with SCI expressed a need for emotional counselling; of these, only 43% felt that these needs were met. Transportation can also be a significant issue for persons with SCI, with 87% and 73% respectively expressing a need for short- and long-distance transportation. 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 has shown to have a greater reduction in levels of anxiety and depression post treatment compared to a waitlist control group, and these levels were maintained at both 3 and 12 month follow-ups. ICBT was shown to have similar effects to face-to-face CBT. These studies demonstrate that guided ICBT is a safe and effective alternative to face-to-face interventions and it may be beneficial for under serviced populations. Hence, examination of its effectiveness is warranted in the SCI population which faces various psychological and somatic secondary issues. Participants with SCI will receive a 8 week guided ICBT program called the Chronic Conditions Course for persons with SCI. The program is completed over 8 weeks with once a week guidance from a coach. The guided course consists of five lessons, Do It Yourself activities, and case vignettes adapted from persons with SCI. The course also provides guidance and resources on other essential skills for persons with SCI, including communicating with health care professional, managing chronic pain, and sleep hygiene. Psychosocial outcomes will be assessed at baseline, 8 weeks, and at 3 months. Data on intervention usage and satisfaction measures will also be examined through a qualitative interview. Caregivers of participants will be asked to complete self-report measures and a qualitative interview regarding their caregiver burden.

Interventions

BEHAVIORALGuided ICBT for persons with Spinal Cord Injury

An 8-week guided 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 guide with experience delivering ICBT will provide support by email or telephone once a week. The guide will spend approximately 15 minutes per week/per client.

OTHERSurvey

Caregiver burden and mental health will be assessed through online questionnaires.

Sponsors

University of Regina
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* 18 years of age or older * residing in Canada * diagnosed with spinal cord injury * 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 Canada during treatment * concerns about online therapy

Design outcomes

Primary

MeasureTime frameDescription
Change in depressionbaseline, start of each Lesson 2-5, 8 weeks, 3 monthsPatient Health Questionnaire - 9 Item (PHQ-9). Higher total scores indicate greater severity of depression. Scores range from 0 to 27.
Change in anxietybaseline, start of each Lesson 2-5, 8 weeks, 3 monthsGeneralize Anxiety Disorder - 7 Item (GAD7). Higher total scores indicate greater severity of anxiety. Scores range from 0 to 21
Change in Caregiver Burden from baseline to 8 weeks (Caregivers of persons with SCI only)baseline, 8 weeksCaregiver burden questionnaire. The tool has 12 items. Total scores ranging from 0 to 18. Higher scores indicate greater burden

Secondary

MeasureTime frameDescription
Quality of life (Persons with SCI only)baseline, 8 weeks, 3 monthsSpinal Cord Injury Quality of Life Short Form; SCI-QoL-SF
Quality of Life (Caregivers of persons with SCI only)baseline, 8 weeks, 3 months, 6 months, and 1 year follow upEQ5D
Service usage (Persons with SCI only)baseline, 8 weeks, 3 months
Pain (Persons with SCI only)baseline, 8 weeks, 3 monthsInternational Spinal Cord Injury Pain Basic Data Set v2.0 ISCIPBDS
Pain interference (Persons with SCI only)baseline, 8 weeks, 3 monthsBrief Pain Inventory Short Form; BPI-SF

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026