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
Effectiveness Progress
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
Unbiased ResultsWe believe in providing patients with all the options.
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Conditions
Cancer Related
Treatments