ACTIVE_NOT_RECRUITING

HOme-Based Self-management and COgnitive Training CHanges Lives (HOBSCOTCH)-Parkinson's Disease (HOBSCOTCH-Parkinson's)

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

The goal of this pilot study is to assess the feasibility of adapting and delivering the existing home-based epilepsy self-management intervention, HOBSCOTCH, for people with Parkinson's Disease (PD) The main questions it aims to answer are: 1. Can the current HOBSCOTCH program be adapted for people with PD? 2. Will people with PD experience improved quality of life similar to that found in people with epilepsy after participating in the HOBSCOTCH program? Participants will be asked to: * attend nine, one-hour virtual (online and/or by telephone) HOBSCOTCH-PD sessions with a one-on-one certified HOBSCOTCH-PD coach * complete a brief clinical questionnaire about their diagnosis of PD * complete two questionnaires before and after the HOBSCOTCH-PD sessions about their quality of life and about memory and thinking processes * keep a short daily diary about their PD symptoms and use of the self-management strategies taught in the HOBSCOTCH-PD program * complete a brief Satisfaction Survey after the entire HOBSCOTCH-PD program

Official Title

HOme-Based Self-management and COgnitive Training CHanges Lives (HOBSCOTCH)-Parkinson's Disease (HOBSCOTCH-Parkinson's)

Quick Facts

Study Start:2024-01-05
Study Completion:2026-07-30
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:ACTIVE_NOT_RECRUITING

Study ID

NCT06260228

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:30 Years to 75 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Age 30 - 75 years
  2. * Diagnosis of Parkinson's Disease per participant's provider
  3. * Literate, English-speaking with grade 12 or equivalent in education
  4. * Self-reported cognitive/memory difficulties
  5. * Telephone and internet access
  1. * Cognitive dysfunction that precludes participation in giving informed consent
  2. * Significant visual impairment precluding reading or writing
  3. * No reliable telephone or internet access

Contacts and Locations

Principal Investigator

Elaine T Kiriakopoulos, MD, MPH, MSc
PRINCIPAL_INVESTIGATOR
Dartmouth-Hitchcock, Dartmouth College

Study Locations (Sites)

Dartmouth-Hitchcock
Lebanon, New Hampshire, 03756
United States

Collaborators and Investigators

Sponsor: Dartmouth-Hitchcock Medical Center

  • Elaine T Kiriakopoulos, MD, MPH, MSc, PRINCIPAL_INVESTIGATOR, Dartmouth-Hitchcock, Dartmouth College

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 Date2024-01-05
Study Completion Date2026-07-30

Study Record Updates

Study Start Date2024-01-05
Study Completion Date2026-07-30

Terms related to this study

Keywords Provided by Researchers

  • Parkinson Disease
  • Memory
  • Cognitive Training
  • Self-Management

Additional Relevant MeSH Terms

  • Parkinson Disease
  • Cognitive Dysfunction
  • Memory Disorders