RECRUITING

Healthy Living After Knee Replacement

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Conditions

ArthroplastyOverweight and Obesity

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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 this study is to examine if a weight loss program designed for adults after knee replacement improves weight loss, physical activity, pain, and function, as well as if the program is cost effective, as compared to a chronic disease self-management program.

Official Title

Physical Activity and Weight Loss to Improve Function and Pain After Total Knee Replacement

Quick Facts

Study Start:2022-01-04
Study Completion:2026-06-30
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05190666

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:Not specified
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:CHILD, ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * have a body mass index between 25-45 kg/m2
  2. * have had a knee replacement (including primary, staged or independent bilateral, or revision) \<6 months prior to baseline assessment
  3. * have a computer, tablet, or smartphone with active internet access to self-monitor online and/or have a device or computer compatible with Fitbit
  4. * completion of baseline assessment measures (height, weight, function tests, surveys, ≥4 days valid of activity monitoring, and 1 day of dietary recall)
  5. * be English-speaking and able to read consent and study materials written in English
  6. * be willing to attend 4 in-person assessments.
  1. * have any contraindications to diet or weight loss
  2. * undergo simultaneous bilateral knee replacement or have a scheduled or anticipated knee replacement for the contralateral knee within the next 18 months
  3. * have a mobility limiting comorbidity unrelated to knee replacement (e.g. spinal stenosis, fibromyalgia, peripheral vascular disease, stroke)
  4. * are taking anti-obesity medications
  5. * are enrolled in a formal weight loss program
  6. * had or are planning to have bariatric/gastric/lap band surgery
  7. * are planning to relocate out of the Columbia or Greenville, SC areas in the next 18 months.

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 Date2022-01-04
Study Completion Date2026-06-30

Study Record Updates

Study Start Date2022-01-04
Study Completion Date2026-06-30

Terms related to this study

Additional Relevant MeSH Terms

  • Arthroplasty
  • Overweight and Obesity