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Combined Effects of PNF and Electrical Muscle Stimulation on Spasticity and Hand Function in Stroke Patients.

R

Riphah International University

Status

Completed

Conditions

Proprioceptive Disorders
Balance; Distorted
Stroke

Treatments

Other: experimental group
Other: control group

Study type

Interventional

Funder types

Other

Identifiers

NCT05916872
REC/RCR & AHS/23/0211

Details and patient eligibility

About

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

Full 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.

Enrollment

30 patients

Sex

All

Ages

30 to 70 years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

30 participants in 2 patient groups

experimental group
Experimental group
Description:
patients in this group will receive contract relax exercises along with EMS
Treatment:
Other: experimental group
control group
Active Comparator group
Description:
patients in groups B will receive conventional therapy.
Treatment:
Other: control group

Trial contacts and locations

1

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Central trial contact

Zeest Hashmi, MS NMPT; Imran I Amjad, PhD

Data sourced from clinicaltrials.gov

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