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NCT04845542Active, not recruiting

Promoting Resilience in Stroke Survivor-carepartner Dyads (ReStoreD)

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

Source: ClinicalTrials.gov · Last updated 30 Jan 2026

Brief summary (registry, in English)

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.

Status (registry)
Active, not recruiting
Study type
Interventional
Enrollment
400 (estimated)
First submitted
12 Apr 2021
Start date
20 Jul 2022
Primary completion date
31 Aug 2026
Lead sponsor
University of Utah
Diseases
Stroke
NCT number
NCT04845542

What you commit to

  • Study type: Interventional
  • Planned participants: 400
  • From 20 Jul 2022 to the primary completion date, 31 Aug 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Either dyad partner has significant aphasia (difficulties with speech), visual, psychiatric, and/or significant cognitive impairment that would limit their ability to participate in the intervention in a meaningful way

Who the study is looking for

  • Community-dwelling cohabitating couple where one partner has a had an ischemic or hemorrhagic stroke
  • The stroke must have occurred between 3 months and 3 years prior to enrollment
  • The adult couple must have been living together since before the stroke and for at least 6 months prior to enrollment
  • One or both partners must report some anxiety and/or depressive symptoms
  • Participants must be able to read, understand, and follow instructions, and be able to provide their own consent

Age in the registry: 18 years to - · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University of Utah
Coordinator of this site? Confirm its status
Salt Lake CityUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.