Skip to main content
Clinical Trials/CTRI/2024/04/065445
CTRI/2024/04/065445Not yet recruitingPhase 3

Effectiveness Of Resistance Training With Task Oriented Training And Resistance Training Alone In Reducing Bradykinesia Of Upper Extremity In Parkinsons Individuals.

Preethi S1 site in 1 country20 target enrollmentStarted: April 16, 2024Last updated:

Trial Snapshot

Phase
Phase 3
Status
Not yet recruiting
Sponsor
Enrollment
20
Locations
1
Primary Endpoint
Improvement in Bradykinesia

Study Overview

Brief Summary

EFFECTIVENESS OF RESISTANCE TRAINING WITH TASK ORIENTED  TRAINING  AND RESISTANCE TRAINING ALONE IN REDUCING BRADYKINESIA  OF UPPER EXTREMITY  IN PARKINSON’S INDIVIDUALS

INTRODUCTION

Parkinson’s disease is a neurodegenerative disease that is  caused by dopamine deficiency in the basal ganglia leading to movement disorder that is characterized by classical Parkinson’s motor  symptoms.

Parkinson’s disease is very common overall ,ranking second among age related degenerative brain diseases. incidence rate is 1.5 times higher at nearly 90,000 cases annually.

Most people diagnosed with Parkinson’s are age 50 years or older.  .The most characteristic motor symptoms  are Bradykinesia, Rigidity,tremor and postural instability.

Bradykinesia  is one of the cardinal symptom of Parkinson’s disease .Upto 98% of all people with Parkinson’s disease experience slowness of movement.

AIM

The study could focus on measuring changes in bradykinesia of upper limb .The goal is to determine which approach lead to more significant improvements in these Parkinson’s individuals-specific symptoms.

OBJECTIVE

To compare the effectiveness of two intervention approaches - Resistance training  with  task oriented training and resistance training alone in reducing bradykinesia in upper extremity of Parkinson’s individuals.

METHODOLOGY

20 patients were divided into 2 groups  group 1 -task oriented training and resistance training   group 2 - resisted training alone training course will last for 6 Weeks,treated for 1 hour per session,thrice a week.

RESULTS

Statistical analysis will be done after data collection and conclusion will be drawn

Study Design

Study Type
Interventional
Allocation
Other
Masking
None

Eligibility Criteria

Ages
50.00 Year(s) to 60.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • Both gender Aged between 50 to 60 years Subjects under medications Hoehn and Yahr scale 2 to 3 Manual Muscle Testing grading 4 and 5 Cooperative and willing to participate Able to follow the instructions.

Exclusion Criteria

  • Unstable vital signs Intentional tremor patients Cognitive impairment Mini Mental Scale Examination greater than 24 Other neurological and orthopedic conditions History of conventional surgery or deep brain stimulation for PD Peripheral neuropathy with motor impairment Hearing and visual impairment.

Outcomes

Primary Outcomes

Improvement in Bradykinesia

Time Frame: At baseline and after 6 weeks

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Preethi S
Sponsor Class
Other [self]
Responsible Party
Principal Investigator
Principal Investigator

Preethi S

Sri Ramakrishna Institute of Paramedical Sciences

Study Sites (1)

Loading locations...

Similar Trials