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NCT06736795 · ClinicalTrials.gov registry record · NA
Progressive Achilles Loading Via Clinician E-support
A NA study of Achilles Tendinopathy and Achilles Tendon Pain, sponsored by Ruth Chimenti.
- Recruiting
- Registry status
- NA
- Development phase
- 160
- Enrollment target
- 2
- Study locations
NCT06736795 is a NA study of Achilles Tendinopathy and Achilles Tendon Pain that is actively recruiting participants, run by Ruth Chimenti. The registered enrollment target is 160 participants, above the 90-participant average among 3 other Achilles Tendinopathy trials with a reported enrollment target (78% higher). The trial reports 2 study locations across 2 states.
The verdict
NCT06736795, a NA study of Achilles Tendinopathy and Achilles Tendon Pain, is actively recruiting participants, sponsored by Ruth Chimenti.
- RECRUITING
- Registry status
- NA
- Development phase
- 160 participants
- Enrollment target
- 2
- Study locations
Study Summary
This is a randomized controlled trial with individuals who have Achilles tendon pain. This study is designed to identify an effective rehabilitation program for Achilles tendon pain that expands access to care for military personnel and to predict treatment response. Limited or delayed access to healthcare can exacerbate the severity of pain and duration of disability due to AT. This is particularly relevant for individuals deployed to battlefield settings or are being seen in busy military treatment facilities. Therefore, it is crucial to identify efficient and effective treatment pathways that maximize healthcare access and facilitate a rapid and pain-free return to full duty.
Conditions Studied
Interventions
- OTHER Exercise
- OTHER Education
Study Locations (2)
Iowa
- University of Iowa Health Care - Gait Analysis Laboratory - Iowa City
Texas
- Carl R. Darnall Army Medical Center (CRDAMC) - Fort Cavazos
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 160 participants |
| Start Date | 2025-08-20 |
| Est. Completion | 2028-07 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06736795
The ClinicalTrials.gov registry entry for NCT06736795 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 160 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 90-participant average among 3 other Achilles Tendinopathy trials with a reported enrollment target (78% higher). The listed sponsor is Ruth Chimenti, which has 4 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Achilles Tendinopathy appearing as the primary indexed condition, and to 2 interventions - of which Exercise is the first listed.
NCT06736795 reports 2 study locations spanning 2 distinct geographic areas - top geographies include Iowa, Texas.
Frequently Asked Questions
What is clinical trial NCT06736795 about?
NCT06736795 is a clinical study titled "Progressive Achilles Loading Via Clinician E-support". This is a randomized controlled trial with individuals who have Achilles tendon pain. This study is designed to identify an effective rehabilitation program for Achilles tendon pain that expands access to care for military personnel and to predict treatment response. Limited or delayed access to hea...
What is the current status of trial NCT06736795?
This trial is currently recruiting. It is a NA study. The enrollment target is 160 participants. The study started on 2025-08-20. Estimated completion is 2028-07.
What conditions does trial NCT06736795 study?
This clinical trial studies the following conditions: Achilles Tendinopathy, Achilles Tendon Pain.
What interventions are being tested in trial NCT06736795?
The interventions under investigation include: Exercise (OTHER), Education (OTHER).
Who is sponsoring clinical trial NCT06736795?
This trial is sponsored by Ruth Chimenti, which has 4 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06736795 being conducted?
This trial has 2 study locations across Iowa, Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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