RECRUITING

Enhancing Purpose and Well-Being Through a Volunteering Experience Connecting Veterans With English Language Learners

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 study is to refine and test a strategy for engaging Veterans with symptoms of depression, anxiety, and/or PTSD (Post Traumatic Stress Disorder) as volunteers to help English language learners (ELLs) improve their speaking skills via structured conversations using videoconferencing.

Official Title

Enhancing Purpose and Well-Being Through a Volunteering Experience Connecting Veterans With English Language Learners

Quick Facts

Study Start:2024-04-15
Study Completion:2025-04-15
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06324383

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. * 18 years of age or older
  2. * fluent English speakers
  3. * diagnosis of depression, anxiety, or PTSD in their outpatient record in the last 12 months.
  4. * be able to participate in a videoconference via a smartphone, tablet, laptop, or desktop computer in their home using a widely-accessible, no cost videoconferencing platform.
  1. * schizophrenia
  2. * dementia
  3. * traumatic brain injury that significantly impedes ability to participate in sessions
  4. * significant sensory impairment
  5. * current alcohol or drug abuse/dependence that would affect their ability to participate in the study

Contacts and Locations

Study Contact

Sarah H Yon, MPH
CONTACT
734-222-7671
shlim@umich.edu

Principal Investigator

John D Piette, PhD
PRINCIPAL_INVESTIGATOR
University of Michigan

Study Locations (Sites)

Center for Clinical Management Research (CCMR), North Campus Research Complex
Ann Arbor, Michigan, 48109
United States

Collaborators and Investigators

Sponsor: University of Michigan

  • John D Piette, PhD, PRINCIPAL_INVESTIGATOR, University of Michigan

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 Date2024-04-15
Study Completion Date2025-04-15

Study Record Updates

Study Start Date2024-04-15
Study Completion Date2025-04-15

Terms related to this study

Additional Relevant MeSH Terms

  • Depression
  • Anxiety
  • Post Traumatic Stress Disorder