ACTIVE_NOT_RECRUITING

Living Longer and Stronger With Spinal Cord Injury (SCI)

Talk to us

Conditions

Spinal Cord Injuriesspinal cord injuryaginghealth promotioninterventionrandomized controlled trial

Quick Navigation

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

The purpose of this study is to develop a health promotion group intervention to meet the unique health promotion needs of people aging with SCI, to test the efficacy of the adapted intervention program, Living Longer and Stronger with SCI, in a randomized controlled trial and to assess the mechanisms through which the intervention may enhance physical, psychological, and social health.

Official Title

Living Longer and Stronger With Spinal Cord Injury: An Online Program for Promoting Healthy Aging

Quick Facts

Study Start:2024-02-13
Study Completion:2026-07-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:ACTIVE_NOT_RECRUITING

Study ID

NCT06227000

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * traumatic spinal cord injury (SCI)
  2. * have traumatic SCI for at least 15 years OR be over the age of 45
  3. * use a manual or power wheelchair for mobility at least some of the time
  4. * reside in the U.S.
  5. * speak and read English
  6. * access to a smart phone, tablet, or a computer with Internet access
  7. * have or be willing to obtain email for study correspondence
  1. * cognitive impairment that significantly limits their ability to give informed consent, participate in the intervention, or complete study assessments as determined by an inability to correctly answer questions demonstrating study comprehension
  2. * have a significant visual or hearing impairment that would prohibit their ability to participate in the interactive online intervention with accommodations
  3. * report active suicidality or significant problems with alcohol or other drug use
  4. * live in an institution

Contacts and Locations

Principal Investigator

Susan Robinson-Whelen, PhD
PRINCIPAL_INVESTIGATOR
The University of Texas Health Science Center, Houston

Study Locations (Sites)

TIRR Memorial Hermann Spinal Cord Injury and Disability Research Center
Houston, Texas, 77030
United States

Collaborators and Investigators

Sponsor: The University of Texas Health Science Center, Houston

  • Susan Robinson-Whelen, PhD, PRINCIPAL_INVESTIGATOR, The University of Texas Health Science Center, Houston

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-02-13
Study Completion Date2026-07-01

Study Record Updates

Study Start Date2024-02-13
Study Completion Date2026-07-01

Terms related to this study

Keywords Provided by Researchers

  • spinal cord injury
  • aging
  • health promotion
  • intervention
  • randomized controlled trial

Additional Relevant MeSH Terms

  • Spinal Cord Injuries