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NCT07148700Completed

Which Tools Better Predict Fall Risk in Parkinson's Disease: A Comparative Study of Objective, Self-Reported, and Functional Balance Assessment

Source: ClinicalTrials.gov · Last updated 9 Jul 2026

Brief summary (registry, in English)

Introduction: Falls are common in Parkinson's disease (PD), affecting 30-90% of patients annually, with more than half experiencing recurrent falls. Identifying balance assessment tools that are both practical and predictive of fall risk is therefore essential. This study aimed to investigate the relationship between fall frequency and three balance assessment tools: the Biodex Balance System (objective), the Falls Efficacy Scale-International (FES-I) (self-reported), and the Mini-Balance Evaluation Systems Test (Mini-BESTest) (functional). Methods: Patients with PD at Hoehn and Yahr stages 1-3 will be included in the study. Fall data will be collected using a fall diary, while objective balance will be assessed with the Biodex Balance System, functional performance will be evaluated with the Mini-BESTest, and self-reported balance confidence will be measured with the FES-I.

Status (registry)
Completed
Study type
Observational
Enrollment
40 (actual)
First submitted
21 Aug 2025
Start date
1 May 2025
Primary completion date
25 Aug 2025
Lead sponsor
Bezmialem Vakif University
NCT number
NCT07148700

What you commit to

  • Study type: Observational
  • Participants enrolled: 40
  • From 1 May 2025 to the primary completion date, 25 Aug 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Presence of visual, hearing impairments, cardiovascular or pulmonary diseases that could affect study outcomes
  • Clinically unstable condition within the past month

Other

  • Having mental or physical impairments severe enough to hinder communication
  • Participation in a rehabilitation program within the last six months

Who the study is looking for

  • Age between 40 and 80 years old
  • Receiving stable dopaminergic treatment
  • No other neurological disorders besides PD
  • A Standardized Mini-Mental State Examination (MMSE) score \>24
  • Hoehn and Yahr stage between 1-3
  • Voluntarily agreed to participate in the study after receiving detailed information

Age in the registry: 40 years to 80 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Bezmialem Vakif University
Coordinator of this site? Confirm its status
IstanbulTurkey (Türkiye)Unknown status

This page is information, not medical advice. Discuss any trial with your doctor.