RECRUITING

Promoting Resilience in Stroke Survivor-carepartner Dyads (ReStoreD)

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

Affecting nearly 800,000 people in the US every year, stroke is a leading cause of long-term disability, and has serious consequences for stroke survivors and their carepartners. Our project uses a scientifically rigorous efficacy study to evaluate a remotely delivered 8-week dyadic (couples-based) positive psychology intervention to reduce emotional distress in stroke survivors and their carepartners. If successful, couples may be better emotionally equipped to cope with the sequelae of stroke, and have better rehabilitation outcomes and quality of life.

Official Title

Testing Efficacy of an Intervention to Promote Resilience in Stroke Survivor-carepartner Dyads (ReStoreD)

Quick Facts

Study Start:2022-07-20
Study Completion:2027-08-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT04845542

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. * Community-dwelling cohabitating couple where one partner has a had an ischemic or hemorrhagic stroke
  2. * The stroke must have occurred between 3 months and 3 years prior to enrollment
  3. * The adult couple must have been living together since before the stroke and for at least 6 months prior to enrollment
  4. * One or both partners must report some anxiety and/or depressive symptoms
  5. * Participants must be able to read, understand, and follow instructions, and be able to provide their own consent
  1. Pregnancy or breastfeeding
  2. Severe psychiatric disorders
  3. Active substance abuse
  4. Unstable medical conditions
  5. Inability to comply with study requirements

Contacts and Locations

Study Contact

Alexandra L Terrill, PhD
CONTACT
8015815951
alex.terrill@hsc.utah.edu
Lorie Richards, PhD, OTR/L
CONTACT
8015851069
lorie.richards@hsc.utah.edu

Principal Investigator

Alexandra L Terrill, PhD
PRINCIPAL_INVESTIGATOR
University of Utah

Study Locations (Sites)

University of Utah
Salt Lake City, Utah, 84108
United States

Collaborators and Investigators

Sponsor: University of Utah

  • Alexandra L Terrill, PhD, PRINCIPAL_INVESTIGATOR, University of Utah

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 Date2022-07-20
Study Completion Date2027-08-31

Study Record Updates

Study Start Date2022-07-20
Study Completion Date2027-08-31

Terms related to this study

Additional Relevant MeSH Terms

  • Stroke
  • Depression, Anxiety
  • Coping Skills
  • Couples