Skip to content

Efficacy of an Evidence-based Telehealth Intervention in Modifying Health Behavior

Efficacy of an Evidence-based Telehealth Intervention in Modifying Health Behaviors Associated With Post-Traumatic Osteoarthritis

Status
Active, not recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07187024
Acronym
MIRROR_14
Enrollment
65
Registered
2025-09-22
Start date
2020-07-24
Completion date
2026-09-01
Last updated
2025-09-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Knee Injuries, Knee Sprain, Post-traumatic Osteoarthritis

Keywords

Telehealth, Behavioral Intervention, PTOA

Brief summary

The overall objective of this study is to evaluate the efficacy of the mare telehealth intervention platform and the intervention on patients' readiness to manage osteoarthritis and patient reported outcomes. To accomplish the stated objectives the investigators will conduct a randomized controlled trial. The independent variable will be group (Intervention vs. Control) and the dependent variables will be patient reported knee status (SA1) and readiness to manage arthritis measures (SA2a), as well as activity level (SA2b). We will also compare knowledge about post-traumatic osteoarthritis (PTOA) between groups prior to and following the intervention (SA3).

Detailed description

The Specific Aims of this project are: Specific Aim 1: Compare the change in patient reported outcomes for knee pain, knee symptoms, and lack of vigorous knee function, from pre-intervention to immediately post-intervention and 6 and 12 months post-intervention, between the intervention group and the control group. Hypothesis 1: From pre-intervention to post-intervention and 6 and 12 months post-intervention, significant decreases in knee pain, knee symptoms, and lack of vigorous knee function will be observed in the intervention group. However, there will be no significant decreases in these outcomes for control participants. Specific Aim 2: Compare the proportion of participants that demonstrate changes on intermediate outcomes (increased readiness to manage PTOA and decreased knee loads from discretionary physical activity), from pre-intervention to immediately post-intervention and 6 and 12 months post-intervention, between the intervention group and the control group. Hypothesis 2a: The proportion of participants that demonstrate an improvement in readiness to manage PTOA risk factors, as indicated by a one-step change on the Readiness to Manage Arthritis Questionnaire, will be significantly higher in the intervention group than in the control group, at 6 and 12 months post-intervention. Hypothesis 2b: Intervention participants will demonstrate a reduction in recreational activities that place high load on the knee, as indicated by a mean decrease on Marx Activity Scale, that will be significantly larger than any decrease in the control group, immediately post-intervention and at 6- and 12-months post-intervention. Specific Aim 3: Compare knowledge about osteoarthritis (OA) risk factors between groups pre- and post-intervention. Hypothesis 3: The proportion of participants that demonstrate knowledge of osteoarthritis pre- and post-intervention will significantly increase in the intervention group compared to the control group post-intervention.

Interventions

BEHAVIORALmCare PTOA Intervention

The mCare PTOA intervention includes five evidence-based modules that focus on 1) basic joint health following injury, 2) self-management strategies, 3) weight management, 4) physical activity, and 5) occupational management. These educational modules will serve as the primary intervention in this study.

Sponsors

University of North Carolina, Chapel Hill
CollaboratorOTHER
Uniformed Services University of the Health Sciences
CollaboratorFED
Keller Army Community Hospital
Lead SponsorFED

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 54 Years
Healthy volunteers
No

Inclusion criteria

* Current or former United States Military Academy (USMA) cadet or active duty service member who has had at least one Anterior Cruciate Ligament (ACL) surgery

Exclusion criteria

* Do not have access to a personal mobile device (tablet or smart phone) * Are less than 6 months post-surgery * Known deployment within the next 12 months that would remove them from connectivity with a telehealth application for more than 3 months * Have not been cleared for full unrestricted return to activity/duty post ACL reconstruction

Design outcomes

Primary

MeasureTime frameDescription
Knee Functionpre-intervention, immediately post-intervention (~6-weeks), 6-months Post Intervention, 12 months post interventionKnee Injury and Osteoarthritis Outcome Score (KOOS)
Readiness to Manage Arthritispre-intervention, immediately post-intervention (~6 weeks), 6 months post-intervention, 12 months post-interventionReadiness to Manage Arthritis Questionnaire

Secondary

MeasureTime frameDescription
Physical Activitypre-intervention, immediately post-intervention (~ 6-weeks), 6 months post-intervention, 12 months post-interventionMarx Activity Rating
OA Knowledgepre-intervention and immediately post-intervention (~6-weeks)OA Knowledge

Other

MeasureTime frameDescription
Knee Functionpre-intervention, immediately post-intervention (~6-weeks), 6 months post-intervention, 12 months post-interventionWOMAC
Measure of Intermittent and Constant Osteoarthritis Painpre-intervention, immediately post-intervention (~6-weeks), 6 months post-intervention, 12 months post-interventionICOAP (Intermittent and Constant OA Pain)

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026