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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06462560
Other study ID # 1052693
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date April 28, 2024
Est. completion date April 2026

Study information

Verified date June 2024
Source Intermountain Health Care, Inc.
Contact Amelia Millward
Phone 801-507-8095
Email amelia.millward@imail.org
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Recruitment information / eligibility

Status Recruiting
Enrollment 334
Est. completion date April 2026
Est. primary completion date April 2025
Accepts healthy volunteers No
Gender All
Age group 55 Years to 85 Years
Eligibility Inclusion 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 ΒΌ 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 Exclusion Criteria: - 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

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Vivo Online Exercise Program
Virtual online exercise programs conducted by the Vivo team consisting of multiple time a week group live programs
Medbridge Home program
At home exercise program accessed through exercise descriptions and short vidoes

Locations

Country Name City State
United States Intermountain Health Murray Utah

Sponsors (2)

Lead Sponsor Collaborator
Intermountain Health Care, Inc. Impactiv, Inc.

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Primary Endpoint 1 Changes from baseline in number of chair stands done in 30-seconds at 3 and 6 months. 6 months post intervention
Secondary Secondary Endpoint 1 Changes from baseline in WOMAC score at 3 and 6 months. 6 months post intervention
Secondary Secondary Endpoint 2 Changes from baseline in length of time (seconds) to do 1-leg balance stance at 3 and 6 months. 6 months post intervention
Secondary Secondary Endpoint 3 Changes from baseline in seconds to complete the 8-foot up and go at 3 and 6 months. 6 months post intervention
Secondary Secondary Endpoint 4 Changes from baseline in number of knee raises completed in 2-minute knee raise at 3 and 6 months 6 months post intervention
Secondary Secondary Endpoint 5 Changes from baseline in number of arm-curls done in 30 seconds at 3 and 6 months 6 months post intervention
Secondary Secondary Endpoint 6 Changes from baseline in PROMIS-Plus-Osteoarthritis of the Knee (OAK) score at 3 and 6 months 6 months post intervention
Secondary Secondary Endpoint 7 Changes from baseline in exercise self-efficacy scale score at 3 and 6 months 6 months post intervention
Secondary Secondary Endpoint 8 Changes from baseline in quality of life (SF-36 score) at 3 and 6 months 6 months post intervention
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