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Core Strengthening Versus Lower Limb Proprioceptive Neuromuscular Facilitation Techniques in Chronic Stroke Patients

R

Riphah International University

Status

Enrolling

Conditions

Stroke

Treatments

Other: core strengthening exercises
Other: Proprioceptive Neuromuscular Facilitation

Study type

Interventional

Funder types

Other

Identifiers

NCT05707065
REC/RCR&AHS/22/0217

Details and patient eligibility

About

Stroke is a global healthcare issue that causes increased death rates. Good trunk stability is essential for balance and extremity use during daily functional activities and higher-level tasks. The anticipatory activity of trunk muscles is impaired in stroke patients. The trunk is the central column of the body; therefore, proximal trunk control is a prerequisite for distal limb movement control, balance, and functional activities. The purpose of the study is to highlight the most appropriate rehabilitation technique for trunk stability.

Full description

A randomized clinical trial will be performed in which 42 patients with strokes will be included. The data will be collected from Riphah Rehabilitation center Lahore and Ittefaq hospital Lahore. Consecutive sampling technique will be used to collect data. The duration of the study will be 10 months. Trunk impairment scale and berg balance scale will be used as the data collection tool. Data collection will be started after taking informed consent from all the patients. Patients will be allocated to intervention groups by randomization. The patients in group A will be given core strengthening exercise for 4 weeks. The patient in group B will be given PNF exercise for the treatment of trunk for 4 weeks. After data collection analysis of pre and post values will be done by using SPSS version 25.

Enrollment

42 estimated patients

Sex

All

Ages

50 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Chronic stroke patients (6 months to 2 years).
  • Participants with first ever ischemic stroke of right or left half of the body.
  • Participants should be able to walk without support for 10 m.
  • MMSE score is ≥ 24.

Exclusion criteria

  • Participants with recurrent stroke; brainstem or cerebellar stroke or hemorrhagic stroke will be excluded.
  • Patients with speech problem after stroke
  • Patients with other neurological disorders including: Parkinson's disease, multiple sclerosis, epilepsy, etc.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

42 participants in 2 patient groups

core strengthening exercises
Experimental group
Description:
Participants will be positioned in supine. * first stage participants will be taught to activate abdominal wall musculature. They will be initially trained to perform abdominal bracing. * Then positioned in quadruped position and asked to lift alternate arms, gradually progressing to alternate leg lifts and alternate arm/leg raises to activate multifidus. * Then side bridges (side plank) exercise for activation of quadratus lumborum and obliques. * Then asked to perform trunk curls in crook lying, asking them to lift their upper trunk slightly (15°) from the plinth, hold the position for 5 sec. * Perform 30 repetitions of each exercise with 8-sec hold. * Maintain normal diaphragmatic breathing throughout the intervention
Treatment:
Other: core strengthening exercises
Proprioceptive Neuromuscular Facilitation
Experimental group
Description:
* Rhythmic initiation (RI) Patients progressively performed voluntary relaxation, passive movements, active assisted, active resisted movements and than active movements. * Dynamic reversals (slow reversals) Isotonic contractions of first agonists and then antagonists performed against resistance was performed initially. * Stabilizing reversals Isotonic contractions of first agonists, then antagonists against resistance was performed in an alternate way. * Mixture of isotonic (agonist reversals, AR) resisted concentric, contraction of agonist muscles moving with the range was performed progressively following eccentric, lengthening contraction, moving slowing to the start position. . Total 30 min for 3 days a week for a total duration of 4 weeks was set as a optimal time frame duration. Each technique was given for 10 min.
Treatment:
Other: Proprioceptive Neuromuscular Facilitation

Trial contacts and locations

1

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Central trial contact

Imran Amjad, Phd

Data sourced from clinicaltrials.gov

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