COMPLETED

Community Health Worker Assisted Task Specific and Cognitive Therapy at Home With Exposure After Stroke

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

CATCHES is a novel intervention for preliminary testing, integrating Task Specific Therapy at home guided by Community Health Workers (CHW) under supervision of a licensed Physical Therapist (PT) guided by telehealth based Cognitive Behavioral Therapy (CBT) to reduce task specific fears through repetitive exposure and adaptive behavioral activation strategies and facilitate engagement in physical activity. 1. To integrate and establish feasibility of CATCHES intervention. Hypothesis: A multidisciplinary team providing home based TST with exposure therapy tailored to an underserved urban setting will inform a patient-centered behavioral intervention to reduce fear of falling (FOF) among post-acute stroke patients returning home. Feasibility outcomes will include recruitment, retention, and fidelity of implementation. 2. Test effects of the intervention on hypothesized treatment mechanism of fear of falling. Hypothesis: Therapy will reduce task specific fear of falling Primary outcome will be change in Activities-specific Balance Confidence Scale. 3. Explore physical activity measures subjectively and objectively. Exploratory outcomes include pre and post Timed Up and Go test, patient reported outcome surveys and activity as measured by wearable devices.

Official Title

Community Health Worker Assisted Task Specific and Cognitive Therapy at Home With Exposure After Stroke

Quick Facts

Study Start:2024-05-09
Study Completion:2025-05-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:COMPLETED

Study ID

NCT06314308

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:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Aged over 18 years
  2. * Plan for discharge home after stroke and ability to provide consent
  3. * Low balance confidence (Activities-specific Balance Confidence \< 80)
  1. * Modified Rankin Scale \> 2 at time of enrollment
  2. * Severe Stroke (NIH Stroke Scale \> 14 and/or significant aphasia, dysarthria, or cognitive impairment precluding ability to complete study questionnaires as determined by interviewer)
  3. * Legal blindness precluding ability to view infographic or education materials
  4. * Terminal non-cardiovascular illness (life expectancy \< 1 year)
  5. * Co-morbid mental illness requiring hospitalization
  6. * Unavailable for follow-up
  7. * Non-English and non-Spanish speaking

Contacts and Locations

Principal Investigator

Imama A Naqvi, MD, MS
PRINCIPAL_INVESTIGATOR
Columbia University

Study Locations (Sites)

The Neurological Institute of New York, Columbia University
New York, New York, 10032
United States

Collaborators and Investigators

Sponsor: Columbia University

  • Imama A Naqvi, MD, MS, PRINCIPAL_INVESTIGATOR, Columbia University

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 Date2024-05-09
Study Completion Date2025-05-31

Study Record Updates

Study Start Date2024-05-09
Study Completion Date2025-05-31

Terms related to this study

Additional Relevant MeSH Terms

  • Stroke, Acute Ischemic