RECRUITING

Telehealth Assessment and Skill-Building Intervention for Stroke Caregivers (TASK III)

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Conditions

Family CaregiversStroke

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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

Caring for a family member after a stroke can be very difficult and worsen the physical and mental health of untrained caregivers. The TASK III intervention is a unique, comprehensive caregiver intervention program that enables caregivers to develop the necessary skills to manage care for the survivor, while also taking care of their own health.

Official Title

Telehealth Assessment and Skill-Building Intervention for Stroke Caregivers (TASK III)

Quick Facts

Study Start:2022-11-30
Study Completion:2026-08-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05304078

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. * Primary caregiver (family member or significant other providing care for a stroke survivor at home).
  2. * Fluent in the English language (i.e., able to read, speak, and understand English)
  3. * Access to telephone or computer.
  4. * No difficulties hearing or talking by telephone or computer.
  5. * Score 4 or more on a 6-item cognitive impairment screener.
  6. * Willing to participate in 9 calls from a nurse and 5 data collection interviews (Baseline, 8, 12, 24, 52).
  1. * Had not had a stroke.
  2. * Did not need help from the caregiver.
  3. * Resides in a nursing home or long-term care facility.
  4. * Under the age of 18 years.
  5. * Prisoner or on house arrest.
  6. * Pregnant.
  7. * Terminal illness (e.g., late stage cancer, end-of-life condition, renal failure requiring dialysis).
  8. * History of Alzheimer's, dementia, or severe mental illness (e.g., suicidal tendencies, schizophrenia, severe untreated depression or manic-depressive disorder).
  9. * History of hospitalization for alcohol or drug abuse within the past 5 years).

Contacts and Locations

Study Contact

Tamilyn Bakas, PhD, RN
CONTACT
513-558-2254
tamilyn.bakas@uc.edu

Principal Investigator

Tamilyn Bakas, PhD, RN
PRINCIPAL_INVESTIGATOR
University of Cincinnati

Study Locations (Sites)

University of Cincinnati College of Nursing
Cincinnati, Ohio, 45219
United States

Collaborators and Investigators

Sponsor: University of Cincinnati

  • Tamilyn Bakas, PhD, RN, PRINCIPAL_INVESTIGATOR, University of Cincinnati

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 Date2022-11-30
Study Completion Date2026-08-31

Study Record Updates

Study Start Date2022-11-30
Study Completion Date2026-08-31

Terms related to this study

Additional Relevant MeSH Terms

  • Family Caregivers
  • Stroke