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Clinical Trials/NCT06677905
NCT06677905
Recruiting
Not Applicable

SCI&U Peer Health Coaching Program for Individuals Newly Discharged From Inpatient Rehabilitation

University of Toronto2 sites in 2 countries76 target enrollmentFebruary 21, 2025

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Spinal Cord Injury
Sponsor
University of Toronto
Enrollment
76
Locations
2
Primary Endpoint
Emotional Distress Subscale in Health Education Impact Questionnaire
Status
Recruiting
Last Updated
7 months ago

Overview

Brief Summary

The goal of this clinical trial is to learn if the online program and web-based platform for delivery of self-management services to people with spinal cord injury (SCI) called "SCI & U" can support transitions from hospital to the community after injury. Specifically, can providing support from trained peer health coaches via the SCI & U web-based self-management program increase health self-management among those within three years of a spinal cord injury with a planned discharge to or living in the community with SCI for less than two years in the province of British Columbia, Canada or the state of Connecticut, United States.

The main question it aims to answer is:

• Does the SCI & U web-based self-management program lower emotional distress and increase self-efficacy Researchers will compare those who participate in SCI & U with those who receive usual peer support after 6 months to see if the SCI & U program improves self-management knowledge, skills and self-efficacy and decreases secondary complications

Participants will:

  • engage in up to 14 online sessions, each of which lasts about an hour with a peer health coach trained in motivational interviewing, goal setting and brief action planning. During sessions, they may also review resources and create follow up plans on the online platform on health management topics
  • complete an interviewer administered survey at baseline, 6 and 12 months
Registry
clinicaltrials.gov
Start Date
February 21, 2025
End Date
December 31, 2026
Last Updated
7 months ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Susan Jaglal

Professor

University of Toronto

Eligibility Criteria

Inclusion Criteria

  • 18 years and older, with a planned discharge to or living in community with SCI for no more than three years since injury and with the ability to speak and understand English

Exclusion Criteria

  • not a member of or willing to become a member of SCI BC or SCIACT

Outcomes

Primary Outcomes

Emotional Distress Subscale in Health Education Impact Questionnaire

Time Frame: From baseline assessment to 6 months followup

The Emotional Distress construct measures overall negative affect including worry, depression and anger.

Secondary Outcomes

  • Health Directed Activities in Health Education Impact Questionnaire(From baseline assessment to 6 months followup)
  • Positive and Active Engagement in Life in Health Education Impact Questionnaire(From baseline assessment to 6 months followup)
  • Self-monitoring and Insight in Health Education Impact Questionnaire(From baseline assessment to 6 months followup)
  • Constructive Attitudes and Approaches in Health Education Impact Questionnaire(From baseline assessment to 6 months followup)
  • Skill and Technique Acquisition in Health Education Impact Questionnaire(From baseline assessment to 6 months followup)
  • Social Integration and Support in Health Education Impact Questionnaire(From baseline assessment to 6 months followup)
  • Health Services Navigation in Health Education Impact Questionnaire(From baseline assessment to 6 months followup)
  • The Patient Activation Measure - (PAM) Survey(From baseline assessment to 6 months followup)
  • Moorong Self-Efficacy Scale(From baseline assessment to 6 months followup)
  • Secondary Conditions Scale(From baseline assessment to 6 months followup)
  • NIH Toolbox Loneliness Scale(From baseline assessment to 6 months followup)
  • System Usability Scale(From baseline assessment to 6 months followup)

Study Sites (2)

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