RECRUITING

Live and Interactive Fitness Training Program (Vivo Knee OA)

Conditions

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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

Potential participants will be screened at clinic. Patients who meet eligibility criteria will be considered for study. After written informed consent is obtained, participants will complete baseline testing and participants who meet eligibility criteria will be randomized 1:1 to 2 treatment arms: Vivo Arm: Vivo twice a week for 6 months and Usual Care Arm: meet with ATC and given Medbridge home exercise program for 6 months. All participants will be followed for 12 months, and will be assessed at 3-,6-, and 12-months. All participants will complete functional assessments, OA patient reported outcomes measures, quality of life, exercise self-efficacy, and fall risk questionnaires, and health care utilization report at each testing visit. A subset of Vivo participants will be asked satisfaction questions at the 3 and 6 month time points.

Official Title

Improving Physical Function and Quality of Life in Adults With Knee Osteoarthritis Utilizing an Online Live and Interactive Fitness Training Program (Vivo Knee OA)

Quick Facts

Study Start:2024-04-28

Study Completion:2026-04

Study Type:Not specified

Phase:Not Applicable

Enrollment:Not specified

Status:RECRUITING

Study ID

NCT06462560

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:55 Years to 85 Years

Sexes Eligible for Study:ALL

Accepts Healthy Volunteers:No

Standard Ages:ADULT, OLDER_ADULT

Inclusion Criteria	Exclusion Criteria
* 55-85 years of age * Diagnosis of Osteoarthritis within the prior 6 months * Symptomatic OA defined as self-report: * Pain in the knee(s) on most days of the month * Difficulty with at least one of the following because of knee pain: * walking ¼ of a mile * climbing stairs * getting in and out of a car, bath, or bed * rising from a chair * or performing shopping, cleaning, or self-care activities * Radiographic KL grade II-III (using Kellgren and Lawrence criteria) of one or both knees * Physically able to participate in strength training - able to do one chair stand unassisted in order to test change in 30-second chair stand * Ambulatory and community-dwelling * Sedentary or insufficiently active as measured by the PAVS * Access to Wi-Fi in defined exercise space * BMI of 20-34.9 kg/m2 * Document medication specific to OA and knee pain * Willing and able to provide consent	* Neurological conditions causing functional impairments (Parkinson's disease, MS, ALS) * Diagnosis of dementia * Inability to complete ≥1 ADLs without assistance. * Knee surgery in the past 6 months * Severe osteoporosis T-score \< -3.5 * No concurrent enrollment in physical therapy for knee pain * No concurrent enrollment in the Intermountain Arthrofit program * Under the age of 55 or ≥85 * Asymptomatic OA * Not having knee pain or having significant knee pain (WOMAC Pain score of ≤3 or ≥18) * KL Grade 1 or 4 * BMI above 34.9 kg/m2 or ≤20 kg/m2 * Participation in formal strength training more than 30 minutes a week in the past 6 months. * PAVS - Participating in 150 minutes per week of moderate intensity physical activity or 75 minutes of vigorous intensity activity, or an equivalent combination of moderate and vigorous intensity physical activity. * Co-morbid disease that would threaten safety or impair ability to participate in a live and interactive strength training program * Symptomatic or severe coronary artery disease; peripheral vascular disease * Untreated hypertension * Active cancer other than skin cancer

Inclusion Criteria

Exclusion Criteria

* 55-85 years of age
* Diagnosis of Osteoarthritis within the prior 6 months
* Symptomatic OA defined as self-report:
* Pain in the knee(s) on most days of the month
* Difficulty with at least one of the following because of knee pain:
* walking ¼ of a mile
* climbing stairs
* getting in and out of a car, bath, or bed
* rising from a chair
* or performing shopping, cleaning, or self-care activities
* Radiographic KL grade II-III (using Kellgren and Lawrence criteria) of one or both knees
* Physically able to participate in strength training - able to do one chair stand unassisted in order to test change in 30-second chair stand
* Ambulatory and community-dwelling
* Sedentary or insufficiently active as measured by the PAVS
* Access to Wi-Fi in defined exercise space
* BMI of 20-34.9 kg/m2
* Document medication specific to OA and knee pain
* Willing and able to provide consent

* Neurological conditions causing functional impairments (Parkinson's disease, MS, ALS)
* Diagnosis of dementia
* Inability to complete ≥1 ADLs without assistance.
* Knee surgery in the past 6 months
* Severe osteoporosis T-score \< -3.5
* No concurrent enrollment in physical therapy for knee pain
* No concurrent enrollment in the Intermountain Arthrofit program
* Under the age of 55 or ≥85
* Asymptomatic OA
* Not having knee pain or having significant knee pain (WOMAC Pain score of ≤3 or ≥18)
* KL Grade 1 or 4
* BMI above 34.9 kg/m2 or ≤20 kg/m2
* Participation in formal strength training more than 30 minutes a week in the past 6 months.
* PAVS - Participating in 150 minutes per week of moderate intensity physical activity or 75 minutes of vigorous intensity activity, or an equivalent combination of moderate and vigorous intensity physical activity.
* Co-morbid disease that would threaten safety or impair ability to participate in a live and interactive strength training program
* Symptomatic or severe coronary artery disease; peripheral vascular disease
* Untreated hypertension
* Active cancer other than skin cancer

Contacts and Locations

Study Contact

Amelia Millward

CONTACT

801-507-8095

amelia.millward@imail.org

Principal Investigator

Anthony Beutler, MD

PRINCIPAL_INVESTIGATOR

Intermountain Health

Study Locations (Sites)

Intermountain Health

Murray, Utah, 84107

United States

Collaborators and Investigators

Sponsor: Intermountain Health Care, Inc.

Anthony Beutler, MD, PRINCIPAL_INVESTIGATOR, Intermountain Health

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 Date2024-04-28

Study Completion Date2026-04

Study Record Updates

Study Start Date2024-04-28

Study Completion Date2026-04

Terms related to this study

Additional Relevant MeSH Terms

Knee Osteoarthritis