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NCT07475741Recruiting

Exergaming for Improving Upper Limb Functions in Parkinson's Disease

Exergaming With Physical Objects for Upper Limb Rehabilitation in Parkinson's Disease: Effects on Functional Outcome

Source: ClinicalTrials.gov · Last updated 19 May 2026

Brief summary (registry, in English)

Parkinson's Disease commonly results in impaired hand dexterity, reducing a patient's ability to perform activities of daily living. While digital exergaming has been used to encourage physical activity and improve motor function, it often lacks real-world tactile engagement. Integrating physical objects into exergaming known as a phygital approach which may enhance sensorimotor learning and functional carryover. However, its impact on upper limb functional outcomes in PD remains underexplored. Objectives: To assess the effectiveness of exergaming with physical objects on functional outcomes of upper limb rehabilitation in individuals with Parkinson's Disease. Methodology: This randomized controlled pilot study will include 30 individuals with early-stage Parkinson's Disease, recruited through convenience sampling and randomly assigned to either a phygital exergaming group or a control group. Both groups will receive sessions over three monthd (3 sessions/week, 30 minutes each). The phygital group will perform task-based exergaming using both physical objects and digital prompts, while the control group will use digital prompts alone. Functional outcomes will be assessed using the Box and Block Test (BBT), at baseline (day 1) and post intervention 12 weeks. Statistical Analysis: Data will be analyzed using SPSS version 25. Descriptive statistics like gender, stages of diseases etc. will be summarized and described as bar charts and percentages. Within-group differences will be assessed using paired t-tests or Wilcoxon signed-rank tests based on data normality. Between-group comparisons will be conducted using independent t-tests or Mann-Whitney U tests. A p-value of less than 0.05 will be considered statistically significant.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
30 (estimated)
First submitted
5 Mar 2026
Start date
Feb 2026
Primary completion date
Sept 2026
Lead sponsor
University of Health Sciences Lahore
NCT number
NCT07475741

What you commit to

  • Study type: Interventional
  • Planned participants: 30
  • From Feb 2026 to the primary completion date, Sept 2026
  • 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

  • History of suffering from other neurological or musculoskeletal conditions affecting hand use for the exercise
  • Not taking any medicine for systemic illness

Other

  • Advanced stage IV or V
  • Patients with severe cognitive deficits.

Who the study is looking for

  • Early-stage Parkinson's Disease from I-III of Hoehn and Yahr scale
  • Cognitinve Assessment MMSE \>= 24 Score
  • Able to communicate and understand the commands
  • Must be on regular use of Levodopa/carbidopa

Age in the registry: 45 years to 85 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
Punjab institute of Neuroscience Lahore
Coordinator of this site? Confirm its status
LahorePakistanRecruiting

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