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Coaching for Caregivers of Children With Spinal Cord Injury

Not Applicable
Completed
Conditions
Spinal Cord Injuries
Registration Number
NCT03898700
Lead Sponsor
Thomas Jefferson University
Brief Summary

This pilot study has two aims. The first aim is to establish the feasibility of coaching for caregivers of youth with spinal cord injury, and the second aim is to establish methodological procedures for a future multi-center study on the effectiveness of coaching as an intervention for caregivers of youth with spinal cord injury.

Detailed Description

This study addresses the unmet needs of female primary informal caregivers of youth with spinal cord injury. A one-group pre-post treatment design will be used. Consented caregivers will receive coaching via face-to-face or via the phone. Each caregiver will participate in up to 10 coaching sessions. Each coaching session will last up to 90 minutes. Coaching sessions will be audiorecorded and transcribed verbatim. Outcomes of coaching on caregivers' self-identified goals will be assessed using the Canadian Occupational Performance Measure.

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
9
Inclusion Criteria
  • female primary caregiver of youth between 6-13 years of age with traumatic spinal cord injury
  • female primary caregivers have legal guardianship of their child with spinal cord injury
  • speak, read and comprehend English
  • be available for face-to-face coaching
  • have a cell phone with text messaging capabilities, and willing to utilize cell or land line for coaching and data collection
  • able to verbalize changes in their own participation or their child's participation during initial screen
  • written consent
Exclusion Criteria
  • severe mental health condition of female caregiver, as documented in child's medical record or reported to research staff by child's treating MD or medical team member
  • abuses illicit or prescribed substances or alcohol at time of initial screen as documented in child's medical record or reported to research staff by child's treating MD or medical team member

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Primary Outcome Measures
NameTimeMethod
Change in Canadian Occupational Performance Measure (COPM)Baseline - before coaching and repeated at end of 10 coaching sessions (12 weeks from baseline)

Rates self perceived performance and satisfaction with self-identified goals on a 10 point likert scale (1 cannot do, not satisfied; 10 can do without a problem, very satisfied). A 2-point change is considered clinically meaningful.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (2)

Shriners Hospitals for Children

🇺🇸

Philadelphia, Pennsylvania, United States

TIRR Memorial Hermann Rehabilitation Hospital

🇺🇸

Houston, Texas, United States

Shriners Hospitals for Children
🇺🇸Philadelphia, Pennsylvania, United States

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