RECRUITING

CAPABLE Care + Connect

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

In this evaluation scale-up research project, the investigators seek to test an implementation of CAPABLE on the infrastructure of home-based primary care for individuals who may experience social isolation and/or loneliness. These two home-based care programs may improve each other and provide opportunity to further improve quality of life for people living with disabilities and the caregivers. The purpose of this mixed methods study is to adapt and test CAPABLE, an existing evidence-based program, to a new target population with the scalable infrastructure of home-based primary care.

Official Title

CAPABLE Care + Connect: Pilot Feasibility of Implementing CAPABLE Into Homebased Primary Care

Quick Facts

Study Start:2025-08-14
Study Completion:2026-05
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT07123298

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:50 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Any patient currently in JHOME
  2. * At risk for or experiencing social isolation as defined by the Lubben Social Network Scale 6 item score less than or equal 12 points or loneliness as defined by the UCLA Loneliness Scale 3 item score of 6 to 9 points
  3. * Cognitive inclusion criteria Montreal Cognitive Assessment (MOCA) \>23 as determined by referring JHOME study team member provider
  4. * English speaking (measures are standardized in English)
  5. * Ability to participate in an approximately 45-60 min virtual or in person meeting
  6. * Eligible for CAPABLE
  7. * 50 years or older
  8. * Not hospitalized over night more than 4 times in the last 12 months
  9. * Have some difficulty with any ADL
  10. * Cognitively intact
  11. * Live in Baltimore County or Baltimore City
  12. * Not receiving active cancer treatment
  13. * Interested in participating in CAPABLE Care partners will be included if the care partners provide \> 10 hours of care/week
  1. * Terminally ill
  2. * live in long term care setting
  3. * receiving active cancer treatment

Contacts and Locations

Study Contact

Samantha Curriero, MPH
CONTACT
443-417-0888
scurrie6@jh.edu

Principal Investigator

Thomas Cudjoe, MD, MPH, MA
PRINCIPAL_INVESTIGATOR
Johns Hopkins University

Study Locations (Sites)

Johns Hopkins School of Nursing
Baltimore, Maryland, 21205
United States

Collaborators and Investigators

Sponsor: Johns Hopkins University

  • Thomas Cudjoe, MD, MPH, MA, PRINCIPAL_INVESTIGATOR, Johns Hopkins 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 Date2025-08-14
Study Completion Date2026-05

Study Record Updates

Study Start Date2025-08-14
Study Completion Date2026-05

Terms related to this study

Additional Relevant MeSH Terms

  • Social Isolation in Older Adults
  • Social Isolation or Loneliness
  • Social Isolation
  • Quality of Life
  • Disability Physical
  • Homebound Persons