COMPLETED

Healthy Aging Through Movement

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

This study aims to examine the effectiveness of a supervised aerobic exercise program for persons with Opioid Use Disorder (OUD). Participants will be enrolled in a 12-week supervised aerobic exercise intervention.

Official Title

The Potential of Exercise to Reduce Pain and Enhance Mobility in Mid-life Adults Undergoing Opioid Use Treatment

Quick Facts

Study Start:2022-05-11
Study Completion:2025-10-09
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:COMPLETED

Study ID

NCT05772884

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:21 Years to 64 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT
Inclusion CriteriaExclusion Criteria
  1. * Adults must be aged 21-64 years old
  2. * Currently enrolled in OMT (opioid maintenance treatment) or present with at least mild opioid use disorder (endorses at least 2 DSM-V criteria for OUD within a 12-month period),
  3. * Insufficiently physically active (defined as exercising \< 20 minutes 3 times/week
  4. * Able to understand and speak English
  5. * Have a body mass index 18.5-40 kg/m\^2
  6. * Willing and able to visit research center up to one time time/week for 12 weeks
  7. * Participants will undergo a supervised maximal exercise test and physical exam by medical supervisor to be cleared for participation.
  1. * Participants must not have heart disease, or had a stroke, uncontrolled diabetes, thyroid condition an eating disorder
  2. * An uncontrolled major psychiatric condition (e.g., schizophrenia; conditions that are well-controlled, however \[e.g., anxiety controlled through therapy\] will not be exclusionary), or other medical condition(s) that contraindicate exercise; and may not be participating in a structured exercise training or weight loss program.
  3. * Participants cannot be pregnant; pregnancy is exclusionary
  4. * One individual per household may enroll.

Contacts and Locations

Principal Investigator

Meredith S Berry, PhD
PRINCIPAL_INVESTIGATOR
University of Florida

Study Locations (Sites)

University of Florida
Gainesville, Florida, 32611
United States

Collaborators and Investigators

Sponsor: University of Florida

  • Meredith S Berry, PhD, PRINCIPAL_INVESTIGATOR, University of Florida

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 Date2022-05-11
Study Completion Date2025-10-09

Study Record Updates

Study Start Date2022-05-11
Study Completion Date2025-10-09

Terms related to this study

Keywords Provided by Researchers

  • Pain
  • Exercise

Additional Relevant MeSH Terms

  • Opioid Use Disorder