Actively Recruiting

Phase Not Applicable
Age: 40Years - 60Years
All Genders
NCT07428824

Effects Of Functional Action Observation With Auditory Cueing In Stroke Patients

Led by Riphah International University · Updated on 2026-02-24

40

Participants Needed

2

Research Sites

25 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study aims to determine the effects of functional action observation therapy with and without rhythmic auditory cueing on balance and gait in patients with stroke. A randomized clinical trial will be conducted at Ittefaq Hospital Trust, Lahore and Alara Healthcare Clinic. The sample size will be 40. The non-probability convenience sampling methodology will be used to select participants who match the inclusion criteria and the online randomization will be used to further randomize them.Participants will be divided into 2 groups, 20 patients in clinical group and 20 patients in experimental group. While the clinical group will receive traditional therapy, the experimental group will receive Funtional Action Observation Therapy with auditory cueing. For four weeks, the subjects underwent 30 minutes of FAO or general action observation (GAO) instruction five times a week. The outcome measures will include assessments of balance and gait using Berg Balance Scale and Functional Gait Assessment. Assessments will be conducted on patients both before and after the intervention to identify any notable variations in their gait and balance

CONDITIONS

Official Title

Effects Of Functional Action Observation With Auditory Cueing In Stroke Patients

Who Can Participate

Age: 40Years - 60Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 40 to 60 years
  • Male or female patients
  • Stroke occurred 6 months to 2 years ago
  • Ability to sit and stand independently
  • Ability to walk more than 10 meters with or without an assistive device
  • No orthopedic impairments affecting both lower limbs
Not Eligible

You will not qualify if you...

  • MMSE score less than 25
  • History of cancer, cardiovascular, respiratory, or significant musculoskeletal disease
  • Uncorrected vision or hearing problems
  • Hospitalization within the past three months
  • Aggressive behavior changes or emotional instability

AI-Screening

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Trial Site Locations

Total: 2 locations

1

Alara Healthcare Clinic

Lahore, Punjab Province, Pakistan

Actively Recruiting

2

Ittefaq Hospital Trust, Lahore

Lahore, Punjab Province, Pakistan

Actively Recruiting

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Research Team

S

Shirin Kamran, MSPT-NM

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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