ReInventing Yourself after SCI structured group CBT for Spinal Cord Injury

Phase-Based Progress Estimates
1
Effectiveness
1
Safety
Spinal Cord InjuryReInventing Yourself after SCI structured group CBT - Behavioral
Eligibility
18+
All Sexes
What conditions do you have?
Select

Study Summary

This trial is testing whether a 6-week intervention delivered either in-person or through YouTube videos can help improve health outcomes for people with spinal cord injuries.

Eligible Conditions
  • Spinal Cord Injury

Treatment Effectiveness

Study Objectives

1 Primary · 6 Secondary · Reporting Duration: The CD-RISC 10 will be administered at baseline and subsequent follow-up assessments (i.e., 6 weeks, 14 weeks, 22 weeks, 30 weeks, 46 weeks)

Week 46
The Connor-Davidson Resilience Scale (CD-RISC 10) short form- assessing change over time
Week 46
General Anxiety Disorder 7-item (GAD-7)- assessing change over time
Week 46
Generalized Self-Efficacy Scale (GSES)- assessing change over time
Week 46
Moorong Self-Efficacy Scale (MSES) - assessing change over time
Week 46
Participation Assessment with Recombined Tools - Objective (PART-O)- assessing change over time
Week 46
Patient Health Questionnaire - 9 (PHQ-9)- assessing change over time
Week 46
Diener Satisfaction with Life Scale (SWLS)- assessing change over time

Trial Safety

Trial Design

3 Treatment Groups

Indiv
1 of 3
Control
1 of 3
Group
1 of 3

Active Control

Experimental Treatment

281 Total Participants · 3 Treatment Groups

Primary Treatment: ReInventing Yourself after SCI structured group CBT · No Placebo Group · N/A

GroupExperimental Group · 2 Interventions: ReInventing Yourself after SCI structured group CBT, ReInventing Yourself after SCI study-specific workbook · Intervention Types: Behavioral, Behavioral
IndivActiveComparator Group · 2 Interventions: ReInventing Yourself after SCI study-specific workbook, ReInventing Yourself after SCI YouTube videos · Intervention Types: Behavioral, Behavioral
ControlNoIntervention Group · 1 Intervention: Control · Intervention Types:

Trial Logistics

Trial Timeline

Screening: ~3 weeks
Treatment: Varies
Reporting: the cd-risc 10 will be administered at baseline and subsequent follow-up assessments (i.e., 6 weeks, 14 weeks, 22 weeks, 30 weeks, 46 weeks)

Who is running the clinical trial?

Craig HospitalLead Sponsor
35 Previous Clinical Trials
7,878 Total Patients Enrolled
Kessler FoundationOTHER
154 Previous Clinical Trials
10,014 Total Patients Enrolled
University of MichiganOTHER
1,632 Previous Clinical Trials
6,417,097 Total Patients Enrolled
Susan Charlifue, PhDPrincipal InvestigatorCraig Hospital

Eligibility Criteria

Age 18+ · All Participants · 5 Total Inclusion Criteria

Mark “Yes” if the following statements are true for you:
You have a history of spinal cord injury/disorder (SCI/D) at any neurological level.
You are able to speak English.\n
You are able to provide informed consent to participate.\n