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Thermal Spa Programme for Knee Osteoarthritis, 3-Week Study (NCT07534189)

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Summary

The NIH ClinicalTrials.gov registry has registered a prospective cohort study (NCT07534189) evaluating a 3-week thermal spa treatment programme for patients with symptomatic knee osteoarthritis. The study will assess knee joint movement using wearable inertial sensors (Xsens), along with secondary outcomes including pain, physical function, quality of life, and blood transcriptomic profiles. Participants will be evaluated at baseline, post-treatment, and at 3- and 12-month follow-up visits.

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What changed

The NIH registered a new prospective cohort study (NCT07534189) on ClinicalTrials.gov examining the effects of a 3-week thermal spa programme on knee osteoarthritis symptoms. The study will use Xsens wearable inertial sensors to measure knee movement fluidity and gait parameters, with additional assessments of pain, physical function, quality of life, and blood transcriptomic profiles at baseline, post-treatment, and 3- and 12-month follow-ups.

For compliance professionals and clinical operations teams, this registration represents an informational record of an upcoming human subjects research study in the US involving medical device sensors. Researchers and institutional review boards may reference this registration for study coordination, while healthcare providers interested in thermal spa interventions for musculoskeletal conditions may monitor outcomes for future clinical applicability.

Archived snapshot

Apr 16, 2026

GovPing captured this document from the original source. If the source has since changed or been removed, this is the text as it existed at that time.

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Prospective Cohort Study Evaluating a Thermal Spa Programme in Symptomatic Knee Osteoarthritis

N/A NCT07534189 Kind: NA Apr 16, 2026

Abstract

This study evaluates the effects of a 3-week thermal spa treatment on knee joint movement in patients with knee osteoarthritis. Knee movement fluidity and gait parameters will be analyzed during standardized tasks using wearable inertial sensors (Xsens). Secondary outcomes include changes in pain, physical function, physical activity, quality of life, and blood transcriptomic profiles. Assessments will be performed at baseline, after treatment, and at 3- and 12-month follow-up visits.

Conditions: Gonarthrosis

Interventions: X-sens sensor, Transcriptomic, Self-questionnaire

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Last updated

Classification

Agency
NIH
Published
April 16th, 2026
Instrument
Notice
Legal weight
Non-binding
Stage
Final
Change scope
Minor
Document ID
NCT07534189
Docket
NCT07534189

Who this affects

Applies to
Healthcare providers Clinical investigators Patients
Industry sector
6211 Healthcare Providers
Activity scope
Clinical trial registration Medical device research Therapeutic intervention study
Geographic scope
United States US

Taxonomy

Primary area
Healthcare
Operational domain
Clinical Operations
Topics
Medical Devices Public Health

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