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Recruiting NCT07447323

NCT07447323 Thumb Proprioception in Trapeziometacarpal Osteoarthritis

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Clinical Trial Summary
NCT ID NCT07447323
Status Recruiting
Phase
Sponsor Hacettepe University
Condition Trapeziometacarpal Osteoarthritis
Study Type OBSERVATIONAL
Enrollment 100 participants
Start Date 2025-10-23
Primary Completion 2026-03

Eligibility & Interventions

Sex All sexes
Min Age 25 Years
Max Age 75 Years
Study Type OBSERVATIONAL
Interventions
Thumb Proprioception Assessment

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 100 participants in total. It began in 2025-10-23 with a primary completion date of 2026-03.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

This study looks at people who have osteoarthritis at the base of the thumb. It examines how well the thumb can sense its position and movement. The study has three goals: 1. To compare these measurements between people with thumb base osteoarthritis and healthy people. 2. To find out whether this ability changes from milder to more advanced levels of osteoarthritis. 3. To explore whether this ability is related to factors such as basic personal characteristics, thumb/hand muscle strength and hand use, pain and touch sensation, and emotional factors like fear of movement, anxiety, and depression. This is an observational study. No treatment is given. Participants complete thumb measurements and several tests/questionnaires.

Eligibility Criteria

Inclusion Criteria (TMC OA group): * Voluntary participation * Radiographic Eaton-Littler stage I-IV confirmed by an orthopedic specialist * Symptom duration ≥6 months * Age 25-75 years * Pain intensity ≥4/10 on the Visual Analog Scale (VAS) during daily activities at assessment * Ability to actively perform ≥40° palmar abduction * Adequate cognitive capacity to understand and perform study procedures (for participants aged ≥65 years: Montreal Cognitive Assessment \[MoCA\] score ≥21) Inclusion Criteria (Control group): * Voluntary participation * No thumb pain * Age 25-75 years * No clinical signs of TMC OA * Negative provocation tests * Adequate cognitive capacity to understand and perform study procedures (for participants aged ≥65 years: MoCA score ≥21) Exclusion Criteria (TMC OA group): * Inability to abduct the thumb beyond 40° due to severe pain/deformity (especially advanced stage III-IV) * Acute trauma or prior surgery of the hand/wrist * Conservative treatment for hand/thumb pain in the same extremity within the previous 6 months * Current use of anti-inflammatory medication * Peripheral nerve disorders affecting proprioception (e.g., carpal tunnel syndrome, dorsal radial nerve irritation, cervical radiculopathy, double crush syndrome) * Concomitant upper-extremity musculoskeletal disorders (e.g., trigger finger, De Quervain's disease) * Generalized joint hypermobility (Beighton score ≥4) * Neuromuscular, systemic peripheral neuropathic, autoimmune, rheumatic, or infectious diseases * Active malignancy * Neurological conditions affecting pain perception * Visual impairment * Pregnancy Exclusion Criteria (Control group): -Exclusion criteria identical to the TMC OA group

Contact & Investigator

Central Contact

Merve Sümeyye Yılmaz, PT

✉ mervesumeyyeyilmaz@icloud.com

📞 +90 507 843 82 69

Principal Investigator

Çiğdem Ayhan Kuru, PT, PhD

PRINCIPAL INVESTIGATOR

Faculty of Physiotherapy and Rehabilitation, Department of Orthopedic Physiotherapy and Rehabilitation, Hacettepe University, Ankara, Turkey

Frequently Asked Questions

Who can join the NCT07447323 clinical trial?

This trial is open to participants of all sexes, aged 25 Years or older, up to 75 Years, studying Trapeziometacarpal Osteoarthritis. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07447323 currently recruiting?

Yes, NCT07447323 is actively recruiting participants. Contact the research team at mervesumeyyeyilmaz@icloud.com for enrollment information.

Where is the NCT07447323 trial being conducted?

This trial is being conducted at Ankara, Turkey (Türkiye).

Who is sponsoring the NCT07447323 clinical trial?

NCT07447323 is sponsored by Hacettepe University. The principal investigator is Çiğdem Ayhan Kuru, PT, PhD at Faculty of Physiotherapy and Rehabilitation, Department of Orthopedic Physiotherapy and Rehabilitation, Hacettepe University, Ankara, Turkey. The trial plans to enroll 100 participants.

ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: July 2026  ·  Data Methodology