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A study to assess the effect of blended exercise program on rigidity score among Parkinson’s Disease patients attending Neuro OPD at AIIMS, New Delhi.

Not yet recruiting
Conditions
Parkinsons disease,
Registration Number
CTRI/2022/09/045762
Lead Sponsor
AIIMS NEW DELHI
Brief Summary

**Aim of the study:-**

The aim of this study is to study the effectiveness of blended Exercise Program on Rigidity Score of Parkinson’s Disease Patient.OBJECTIVES       Primary objectives 1. To assess and compare the rigidity score among Parkinson’s Patients in both control and intervention group. 2.To assess the effectiveness of blended exercise program on rigidity scores of Parkinson’s patient in Intervention group .         Secondary objectivesTo associate the baseline rigidity scores with selected demographic variables in both intervention and control group.

**HYPOTHESIS**

**H1**: There will be a significant difference in post test rigidity scores among Parkinson’s  patients in control and Intervention group as measured by Unified Parkinson Disease Rating Scale motor score (Part III) at 0.05 level of significance.

 **H2:-** There will be a significant difference in the pre test and post test rigidity scores among Parkinson’s Patient in the Intervention group as measured by Unified Parkinson Disease Rating Scale motor score (Part III) at 0.05 level of significance.

Detailed Description

Not available

Recruitment & Eligibility

Status
Not Yet Recruiting
Sex
All
Target Recruitment
60
Inclusion Criteria
  • Parkinson’s Disease Patients attending Neurology OPD at AIIMS, New Delhi.
  • Patients who are willing to participate in the study.
  • Patients who are able to follow commands and instructions.
  • Patients with Parkinson’s Disease with Hoehn and Yahr stages 2.0,2.5 and 3.0.
Exclusion Criteria
  • •Parkinson’s Disease patients having a clinical diagnosis of dementia (using the Mini-Mental State Examination with a score _ 24/30).
  • •Parkinson’s Disease patients with any clinically significant medical condition, such as cardiopulmonary disease and musculoskeletal problems that could affect gait assessments.
  • •Parkinson’s disease patients with visual problems that could not be corrected with lenses or glasses.
  • •Patient with Parkinson’s Plus Syndrome.
  • •Patients who are not giving consent for the study.
  • •Patients who are not able to communicate in Hindi or English.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To assess rigidity scores of patients using unified Parkinson’s disease rating scale part III6weeks
Secondary Outcome Measures
NameTimeMethod
nana

Trial Locations

Locations (1)

AIIMS, NEW DELHI

🇮🇳

South, DELHI, India

AIIMS, NEW DELHI
🇮🇳South, DELHI, India
REETIKA
Principal investigator
7351958212
reetikarajpura@gmail.com

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