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Clinical Trials/NCT05916872
NCT05916872
Completed
Not Applicable

Combined Effects of Proprioceptive Neuromuscular Facilitation and Electrical Muscle Stimulation on Spasticity and Hand Function in Stroke Patients.

Riphah International University1 site in 1 country30 target enrollmentNovember 1, 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Stroke
Sponsor
Riphah International University
Enrollment
30
Locations
1
Primary Endpoint
Modified Barthel Index:
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

To determine the combined effects of proprioceptive neuromuscular facilitation and electrical muscle stimulation on spasticity and hand function in stroke patients.

Detailed Description

It will be a randomized controlled trial. The stroke patients aged between 30-70 years will be included in this study. Participants will be selected with non-probability convenience sampling technique. Participants will be randomly allocated into two groups by lottery method i.e experimental group and control group. The experimental group will receive proprioceptive neuromuscular technique (contract relax-10 repetition) (5-min) and electrical muscle stimulation(10 min) as 15 min session 3 times a week for four weeks while the control group will receive only conventional therapy. The outcome measure will be calculated by modified barthel index, modified ashworth scale and wolf motor function test.

Registry
clinicaltrials.gov
Start Date
November 1, 2022
End Date
September 15, 2023
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Both ischemic and haemorrhagic stroke patients
  • Chronic stroke patients from 6 month to 2years
  • Mini Mental Scale Examination (MMSE) more than 25

Exclusion Criteria

  • Transient ischemic attack
  • Recurrent stroke
  • Stroke patient with comorbidity and cardiac disease
  • Myopathies

Outcomes

Primary Outcomes

Modified Barthel Index:

Time Frame: 9 months

It is used for assessing the activities of daily living. It is composed of 10 questions that link the degree of independence to daily living activities. Collin et, al; proposed amendment in 1988, in which each domain was scored in one-point increments, ranging from 0 to 2 or 3 for each activity with a maximum score of 20 suggesting functional independence. It is highly reliable and has a good correlation with other disability measures.

Modified Ashworth Scale:

Time Frame: 9 months

Modified Ashworth Scale: It is used to assess the spasticity in patients of stroke or spinal cord injury. Scores range from 0 to 4, where lower scores represent normal muscle tone and higher scores represent spasticity. It is characterized by exaggerated deep tendon reflexes that interfere with muscular activity, gait, movement, or speech. It has excellent validity and reliability.

Study Sites (1)

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