Feasibility of a Mindfulness and Physical Activity Promotion Intervention After Anterior Cruciate Ligament Reconstruction
Public ClinicalTrials.gov record NCT07912502. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.
Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.
Official title
Mind in Motion: Determining the Feasibility of a Mindfulness and Physical Activity Promotion Intervention After Anterior Cruciate Ligament Reconstruction
Brief summary
Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.
The goal of this clinical trial is to learn whether a 6-week mobile-delivered intervention combining mindfulness meditation (Headspace) and personalized, wearable-derived physical activity goals (Oura Ring) can be feasibly delivered to young people who are 1-5 years post-anterior cruciate ligament reconstruction (ACLR) and who have elevated fear of reinjury. The main questions it aims to answer are: * Can the Mind in Motion intervention be implemented with acceptable rates of recruitment, retention, engagement (mindfulness session completion, Oura Ring wear), and participant-rated acceptability? * On days following a completed mindfulness session, do participants report lower anticipated fear of movement and show higher objectively measured moderate-to-vigorous physical activity (MVPA), compared with other days? Participants will: * Complete two brief in-person visits (approximately 1 week apart) that frame a 6-week home-based intervention period, followed by a remote assessment 4 weeks after the intervention ends. * Wear a research-grade activPAL accelerometer on the thigh for 7 days before and 7 days after the intervention to measure objective physical activity. * During the 6-week intervention, complete five 10-minute Headspace mindfulness sessions per week, wear an Oura Ring daily to receive personalized daily activity goals, and complete brief twice-daily check-ins (ecological momentary assessments) about fear, mood, and activity. * Complete standard questionnaires about injury-related fear, psychological readiness for activity, and knee function/symptoms at baseline, mid-intervention, immediately after the intervention, and at a 4-week follow-up. * Complete a brief audio-recorded exit interview describing their experience with the intervention. This is a single-arm, single-site feasibility study; there is no control group and no randomization. Findings will inform the design of a future multisite randomized controlled trial.
Study identification
- NCT ID
- NCT07912502
- Recruitment status
- Not yet recruiting
- Study type
- Interventional
- Phase
- Not applicable
- Enrollment
- 24 participants
Conditions and interventions
Eligibility (public fields only)
- Age range
- 15 Years to 30 Years
- Sex
- All
- Healthy volunteers
- Healthy volunteers not accepted
This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.
Study timeline
- Start date
- Dec 15, 2026 (Estimated)
- Primary completion
- Sep 14, 2027 (Estimated)
- Completion
- Dec 31, 2027 (Estimated)
- Last update posted
- Nov 3, 2026
2026 – 2027
United States locations
- U.S. sites
- 1
- U.S. states
- 1
- U.S. cities
- 1
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| Student Health and Wellness Center | Charlottesville | Virginia | 22901 | — |
Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.
About this trial record page
- What this page shows
- Public field values for ClinicalTrials.gov record NCT07912502, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
- What this page does not do
- No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
- Where the data comes from
- Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
- Last refresh
- Last update posted Nov 3, 2026 · Synced Nov 3, 2026
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Open the official record
The complete public registry record, listed eligibility criteria, and available contact information for NCT07912502 live on ClinicalTrials.gov.