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NCT07422064
Validity and Reliability of the Six-Minute Pegboard Ring Test in Individuals With Parkinson's Disease
trial in Parkinson's Disease (PD) in 47 participants. Completed in 6 February 2026.
15 December 2025
Quick facts
| Lead sponsor | Sanko University |
|---|---|
| Status | Completed |
| Study type | OBSERVATIONAL |
| Enrollment | 47 |
| Start date | 1 November 2025 |
| Primary completion | 15 December 2025 |
| Estimated completion | 6 February 2026 |
| Sites | 1 location across Turkey (Türkiye) |
Conditions studied
- Parkinson's Disease (PD) — all drugs for Parkinson's Disease (PD) →
- Functional Capacity — all drugs for Functional Capacity →
- Upper Extremity Function — all drugs for Upper Extremity Function →
- Validity and Safety — all drugs for Validity and Safety →
Sponsor
Sanko University
Who can join
Adults 35 to 65, any sex, with Parkinson's Disease (PD) or Functional Capacity. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Parkinson's patients who volunteer to participate in the study will be included. Parkinson's patients participating in the study will be referred from the SANKO University Hospital Neurology Outpatient Clinic. The assessments of patients referred from the Neurology Outpatient Clinic will be conducted at the SANKO University Physiotherapy and Rehabilitation Department Research Laboratory. The socio-demographic information of the included patients will be collected. Patients will then be grouped using the Hoehn-Yahr Staging Scale. Vital signs such as blood pressure, saturation, and pulse will be measured. Upper extremity muscle strength will be assessed using a dynamometer. Upper extremity performance will be assessed using the Nine-Hole Peg Test. The patient's fatigue will be assessed using the Fatigue Severity Scale, and upper extremity disability will be assessed using the Disability of the Arm, Shoulder, and Hand (DASH) questionnaire. The assessments will be conducted by Physiotherapist Rüveyda GÜRDAL.Except for the six-minute pegboard ring test, the other tests will evaluate the parameters required for an individual's upper extremity function. These parameters are balance, muscle strength, and fine motor skills. The six-minute pegboard ring test will be reassessed one week later by a different physiotherapist at the SANKO University Department of Physiotherapy and Rehabilitation Research Laboratory.
Publications & conference data
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
Verify or expand the search:
- PubMed search for NCT07422064
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT07422064 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Sanko University
- Last refreshed: 19 February 2026
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07422064.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing