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 with spinal cord injury or disability, and to improve the well being of the spinal cord-injured survivor. In a three-group, randomized, controlled design providing access to information, resources, and support, we predict that the dual target approach will have a greater positive impact on both the caregiver and survivor than the caregiver-only approach, and that both active treatments will be superior with respect to caregiver outcomes than an information-only control condition.

Condition	Intervention
Spinal Cord Injuries	Behavior: Education on effects of SCI  Behavior: Access to local and national SCI-related resources  Behavior: Intervention sessions on physical/social health  Behavior: Peer support group discussions

Further Study Details: 

Primary Outcomes: Mood (survivor and caregiver) (6 and 12 months); Burden (caregiver) (6 and 12 months); Secondary conditions (survivor) (6 and 12 months)
Secondary Outcomes: Knowledge (survivor and caregiver) (6 and 12 months); Social support and social activities (survivor and caregiver) (6 and 12 months); Quality of care (survivor) (6 and 12 months); Safety and mobility (survivor) (6 and 12 months)
Expected Total Enrollment:  432

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 causal linkages between the treatment components (e.g. knowledge, social support) of a multi-component intervention and specific treatment outcomes (e.g. caregiver depression, quality of life).
3. Explore cultural and racial differences in the evaluation of and effectiveness of the different treatment approaches.

Overall, the issues affecting management of SCI/D in later life are complex and hold critical implications for the health of the long-term survivor as well as for those who provide care in the home environment. Large numbers of individuals are living with the effects of SCI/D for decades post-injury. In addition to the health-related complications that typically accompany older age, these individuals are especially vulnerable to co-occurring medical conditions that require high degrees of support and maintenance. Consequently, older caregivers face multiple and often extreme challenges in providing support to the SCI/D survivor at a time in their lives when their own abilities may be compromised due to age-related changes in health and functioning.

The multi-faceted burden faced by caregivers is associated with high levels of depression and anxiety as well as the onset of deleterious physical symptoms. The cumulative effects of such multiple stressors over time all too frequently leave the caregiver unable to continue providing the level of support necessary to maintain their partner’s health in the home environment. In order to circumvent the additional distress certain to accompany such a family separation, Elliott et al. (2001, p. 230) recently concluded that “there is a pressing need for interventions that help family [SCI] caregivers address the routines and tasks essential to maintaining family functioning.”

Ages Eligible for Study:  30 Years and above,  Genders Eligible for Study:  Both

Criteria

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

Please refer to this study by ClinicalTrials.gov identifier  NCT00148239

Amy Lustig, PhD      412-624-2078    alustig@ucsur.pitt.edu

Florida
      University of Miami, Miami,  Florida,  33136,  United States; Recruiting
Pennsylvania
      University of Pittsburgh (UCSUR), Pittsburgh,  Pennsylvania,  15260,  United States; Recruiting

Study chairs or principal investigators

Richard Schulz, PhD,  Principal Investigator,  University of Pittsburgh   

Study ID Numbers:  5 R01 NR08272
Last Updated:  September 6, 2005
Record first received:  September 2, 2005
ClinicalTrials.gov Identifier:  NCT00148239
Health Authority: United States: Institutional Review Board
ClinicalTrials.gov processed this record on 2005-09-13