RECRUITING

Comparative Effectiveness of IIMR Versus CDSMP

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 study will enroll 600 people with serious mental illness who receive services at Centerstone in KY or TN and will compare two different evidence-based self-management interventions: Integrated Illness Management and Recovery (I-IMR), a program developed by the study team at Dartmouth that trains people with serious mental illness on physical and mental health self-management, and the Stanford Chronic Disease Self-Management Program (CDSMP), a program largely focused on physical health self-management that has been used widely in the general population.

Official Title

Comparative Effectiveness of Integrated Illness Management and Recovery Versus the Chronic Disease Self-Management Program

Quick Facts

Study Start:2019-09-02
Study Completion:2027-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT03966872

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. * Serious Mental Illness (diagnosis of schizophrenia, schizoaffective disorder, bipolar disorder, or chronic depression with moderate impairment in functioning) receiving services at Centerstone(KY and TN)
  2. * Diagnosis of a chronic medical condition increasing risk of early mortality from cardiovascular or respiratory disease (e.g., diabetes, hyperlipidemia, hypertension, COPD, heart failure, tobacco dependence, obesity), and at least 1 ER visit or hospitalization within the past year or judgment by the treatment team of substantial need for illness self-management training.
  1. * Consumers who do not speak English
  2. * Consumers with either no, or a well-controlled medical condition will not be included
  3. * Individuals residing in a nursing home or other institution
  4. * Evidence of significant cognitive impairment as indicated by a Mini Mental Status Examination score \<24, will be excluded

Contacts and Locations

Study Contact

Meghan Santos, MSW
CONTACT
603-226-6804
Meghan.M.Santos@Dartmouth.edu
Gail Williams, MS
CONTACT
603-226-6803
Gail.E.Williams@Dartmouth.edu

Principal Investigator

Sarah Pratt
PRINCIPAL_INVESTIGATOR
Dartmouth-Hitchcock Medical Center

Study Locations (Sites)

Seven Counties Services
Louisville, Kentucky, 40220
United States
Centerstone
Nashville, Tennessee, 37228
United States

Collaborators and Investigators

Sponsor: Dartmouth-Hitchcock Medical Center

  • Sarah Pratt, PRINCIPAL_INVESTIGATOR, Dartmouth-Hitchcock Medical Center

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 Date2019-09-02
Study Completion Date2027-01

Study Record Updates

Study Start Date2019-09-02
Study Completion Date2027-01

Terms related to this study

Keywords Provided by Researchers

  • integrated health
  • mental health
  • illness management
  • cardiovascular disease
  • physical health

Additional Relevant MeSH Terms

  • Mental Illness
  • Chronic Disease