RECRUITING

A Hip Flexion Feedback System for Exercise Monitoring in Individuals With Osteoarthritis and Obesity

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

Exercise is very important for living healthier and longer lives. For people with obesity and osteoarthritis, exercise is even more important because it can help them feel less pain in their joints. Also, the more intense the exercise is, the larger the health benefits will be. The most common ways to exercise are running and riding a stationary bicycle. However, these two types of exercise can cause problems for people with obesity and osteoarthritis. Fast running creates large loads in the knees because of the impact of the foot on the ground. On the other hand, studies in cycling show limited improvement in pain because cycling does not allow the feet to move freely, which is important for reducing pain in people with osteoarthritis. This study introduces a new way to exercise using a hip flexion feedback system (HFFS). The subjects will exercise by increasing how much they lift their knees while walking on treadmill. The exercise will also involve controlling the impact of the feet on the treadmill. The HFFS monitors the subject's heart rate during the exercise using a standard heart rate monitor. A TV placed in front of the treadmill shows how high individuals need to lift their knees. How much participants need to lift their knees is calculated by the HFFS based on real-time heart rate readings. Therefore, the HFFS can help people stay at a specific exercise intensity by controlling how high it tells them lift their knees during the exercise. This study will have participants with osteoarthritis and obesity in two groups. One group will exercise using the HFFS. Another group will not exercise. The exercise group will do a 12-week high intensity exercise program. Our first goal is to determine how much fitness, pain, and the ability to move improve due to the exercise program. With this study we are looking to introduce a better and safer way to exercise for people with osteoarthritis and obesity. The results of this study will also allow for further development of home-based exercise and telemedicine.

Official Title

A Hip Flexion Feedback System for Exercise Monitoring in Individuals With Osteoarthritis and Obesity

Quick Facts

Study Start:2023-07-01
Study Completion:2026-03-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05997862

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:30 Years to 75 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Age 30 to 75 years;
  2. * BMI ≥ 30.0 kg/m2 and ≤ 50.0 kg/m2;
  3. * Symptomatic knee OA (defined as a self- report of physician diagnosis of knee OA and current knee symptoms in at least one knee determined from a minimum score of 5 of 20 on the pain subscale of the WOMAC).
  4. * Sedentary (not meeting ACSM guidelines for physical activity)
  5. * Medical clearance for participation
  1. * Self- reported fibromyalgia, rheumatoid arthritis, or other systemic rheumatic disease.
  2. * Severe dementia or other memory loss condition
  3. * Active diagnosis of psychosis or current uncontrolled substance abuse disorder
  4. * Has been hospitalized for a stroke, heart attack, or heart failure, or had surgery for blocked arteries in the past 3 months
  5. * Had a total joint replacement knee surgery, other knee surgery, meniscus tear, or anterior cruciate ligament tear in the past 6 months
  6. * Is on a waiting list for total joint replacement
  7. * Had an intra-articular injection in past 3 months or scheduled during the study period;
  8. * Has severely impaired hearing or speech
  9. * Is pregnant
  10. * Has a serious or terminal illness as indicated by referral to hospice or palliative care
  11. * Resides in a nursing home
  12. * Has any other health problems that would prohibit safe participation in the study

Contacts and Locations

Study Contact

Nuno Oliveira, PhD
CONTACT
601-266-5804
nuno.oliveira@usm.edu
Sam Bruton
CONTACT
601-266-6756
samuel.bruton@usm.edu

Study Locations (Sites)

University Southern Mississippi
Hattiesburg, Mississippi, 39402-7326
United States

Collaborators and Investigators

Sponsor: University of Southern Mississippi

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 Date2023-07-01
Study Completion Date2026-03-31

Study Record Updates

Study Start Date2023-07-01
Study Completion Date2026-03-31

Terms related to this study

Keywords Provided by Researchers

  • Exercise
  • Osteoarthritis
  • Obesity

Additional Relevant MeSH Terms

  • Osteoarthritis, Knee
  • Obesity