Status:

COMPLETED

Health Interventions for Survivors and Primary Support Persons of Spinal Cord Injury

Lead Sponsor:

University of Pittsburgh

Collaborating Sponsors:

University of Miami

Conditions:

Spinal Cord Injuries

Eligibility:

All Genders

30+ years

Phase:

PHASE2

PHASE3

Brief Summary

The overall objective of this project is to test the efficacy of an innovative multi-component intervention aimed at reducing the risk for adverse health outcomes among caregivers of older survivors w...

Detailed Description

The specific aims of this project are to: 1. Assess the impact of a dual target (caregiver and care recipient) intervention compared to a traditional caregiver-only intervention strategy. 2. Assess c...

Eligibility Criteria

Inclusion

  • Inclusion Criteria (Survivors):
  • have adult-onset disability resulting from spinal cord injury, trauma, or disease,
  • be survivors with complete or incomplete injury as defined by the American Spinal Injury Association (ASIA) impairment scale
  • require and use some type of assistance for getting around (e.g., wheelchair, cane, etc.) be 30 years old or older be living at home for a minimum of 1 year post-injury (to avoid the acute trauma phase) speak English.
  • Inclusion Criteria (Caregivers):
  • Is a family member/partner (e.g. spouse, child, or fictive kin)
  • is 18 years of age or older
  • is or is not living with the care recipient
  • speaks English
  • has a telephone at home
  • plans to live in the area for at least 6 months.
  • self-identifies as white, African American or Hispanic.
  • Exclusion Criteria:
  • has a terminal illness with life expectancy of less than 6 months
  • is in active treatment for cancer (except for tamoxifen and lupron)
  • is blind or deaf
  • if the survivor is cognitively impaired due to brain injury or dementia and/or has no use of their hands and severe limitations in speech production

Exclusion

    Key Trial Info

    Start Date :

    September 1 2002

    Trial Type :

    INTERVENTIONAL

    Allocation :

    ACTUAL

    End Date :

    July 1 2008

    Estimated Enrollment :

    380 Patients enrolled

    Trial Details

    Trial ID

    NCT00148239

    Start Date

    September 1 2002

    End Date

    July 1 2008

    Last Update

    December 2 2015

    Active Locations (2)

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    Page 1 of 1 (2 locations)

    1

    University of Miami

    Miami, Florida, United States, 33136

    2

    University of Pittsburgh (UCSUR)

    Pittsburgh, Pennsylvania, United States, 15260