RECRUITING

Dose Response of Exercise for Arthritis Management

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Conditions

ArthritisRheumatoid Arthritis (RA)GoutFibromyalgia (FM)OsteoarthritisLupus Erythematosus, Systemicexercisephysical activity

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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 purpose of the study is to see examine the effects of 3 different levels of physical activity (45 minutes/week, 90 minutes/week, or 150 minutes/week) on arthritis symptoms.

Official Title

Examination of the Dose Response Relationship Between Physical Activity and Arthritis-Attributable Outcomes

Quick Facts

Study Start:2025-04-01
Study Completion:2029-04-30
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06880653

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. * 18 years or older
  2. * Have a doctor diagnosed form of arthritis, rheumatoid arthritis, gout, lupus, or fibromyalgia
  3. * Ability to read and write in English
  1. * Have any contraindications to exercise (besides arthritis)
  2. * Engage in ≥30 min/week of Actigraph assessed MVPA
  3. * Are pregnant, breastfeeding, or planning to become pregnant in the next year
  4. * Are planning to relocate out of the Columbia, SC area in the next 12 months,
  5. * Do not have a device compatible with Fitbit
  6. * Have uncontrolled hypertension (e.g., systolic blood pressure \> 160 mmHg or diastolic blood pressure \> 100 mmHg)
  7. * Plan to have a surgery that affects mobility in the next 12 months
  8. * Have a serious cognitive impairment.
  9. * Not willing to be randomized to any of the 3 conditions, do not believe they could adhere to the goals, or do not believe they could achieve the highest dose of activity (150 minutes/week).

Contacts and Locations

Study Contact

Ellen Wingard
CONTACT
803-777-1889
EWINGARD@mailbox.sc.edu

Principal Investigator

Christine Pellegrini, PhD
PRINCIPAL_INVESTIGATOR
University of South Carolina

Study Locations (Sites)

University of South Carolina
Columbia, South Carolina, 29208
United States

Collaborators and Investigators

Sponsor: University of South Carolina

  • Christine Pellegrini, PhD, PRINCIPAL_INVESTIGATOR, University of South Carolina

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 Date2025-04-01
Study Completion Date2029-04-30

Study Record Updates

Study Start Date2025-04-01
Study Completion Date2029-04-30

Terms related to this study

Keywords Provided by Researchers

  • arthritis
  • exercise
  • physical activity

Additional Relevant MeSH Terms

  • Arthritis
  • Rheumatoid Arthritis (RA)
  • Gout
  • Fibromyalgia (FM)
  • Osteoarthritis
  • Lupus Erythematosus, Systemic