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

Status: Recruiting
Location: See location...
Intervention Type: Combination product, Procedure
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 45
Maximum Age: 85
Healthy Volunteers: f
View:

• 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

Locations
Other Locations
Pakistan
Punjab institute of Neuroscience Lahore
RECRUITING
Lahore
Contact Information
Primary
Hafiz Muddassir Riaz, Ph.D Scholar
muddassir.riaz@gmail.com
+92345-6627409
Time Frame
Start Date: 2026-02-20
Estimated Completion Date: 2026-11
Participants
Target number of participants: 30
Treatments
Active_comparator: Control Group (Conventional Physical Therapy Group)
It will act as control group. The participants in this control group will receive the 36 sessions (three sessions per week over 12 weeks), each lasting approximately 30 minutes).
Experimental: Phygital Group (Exergamig)
The intervention group (phygital) will receive thirty six sessions (three sessions per week over twelve weeks), each lasting approximately 30 minutes, involving structured exergaming tasks using physical objects (e.g., blocks, spoons, cups) combined with digital prompts on a tablet or laptop.
Related Therapeutic Areas
Sponsors
Leads: University of Health Sciences Lahore
Collaborators: Punjab Institute of Neurosciences Lahore

This content was sourced from clinicaltrials.gov