Clinical trial Recruiting at 1 site Interventional Ages 40 to 60

Effects of Task-Oriented Training With and Without Rhythmic Auditory Stimulation in Post-Stroke Patients

Official title: Effects of Task-Oriented Training With and Without Rhythmic Auditory Stimulation on Lower Limb Motor Function, Dynamic Balance, Proprioception, Motivation, and Adherence in Post-Stroke Patients

Run by Riphah International University · NCT07724730 · Data updated 2026-11-12

This study tests whether adding rhythmic auditory cues to task-focused training helps adults 40–60 months after stroke improve lower‑limb function, balance, and proprioception.

Quick facts

Study typeInterventional
Ages40 Years to 60 Years
SexAll
Enrollment38 (estimated)
SponsorRiphah International University
Academic / other
Locations1 site (Daska Kalan)
StatusRecruiting
StartedJune 1, 2025
Main results expectedJuly 30, 2026
Study endsAugust 5, 2026
Registry record updatedJuly 24, 2026
Trial IDNCT07724730 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are adults 40–60 with a first-time subacute ischemic or hemorrhagic stroke within 6 months, able to walk 10 meters with or without minimal assistance, and able to follow simple commands.

Probably not a fit

Patients unlikely to benefit include those with severe aphasia, other major neurological disorders, uncontrolled cardiovascular issues, or medical conditions limiting participation.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

In this single blinded randomized trial, 38 adults aged 40–60 with subacute stroke will be assigned to either Task-Oriented Training plus Rhythmic Auditory Stimulation or Task-Oriented Training alone. Both groups will have supervised 30‑minute sessions five days a week for eight weeks, plus a 30‑minute baseline physiotherapy program. Outcomes include motor function, dynamic balance, proprioception, motivation, and adherence, assessed before and after the intervention using LEFS, TUG, JPS, SRMS, and RAQ. Data will be analyzed with SPSS to determine whether adding rhythmic cues provides additional benefit. The study uses sealed opaque randomization and non-probability convenience sampling.

Why it matters

Potential benefit: If successful, patients may experience greater improvements in leg function, balance, and proprioception, potentially enhancing independence.

How similar studies have gone: Previous work suggests that sensorimotor cueing can enhance rehabilitation, but results vary and this specific combination in subacute stroke is being tested.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* • Age 40-60 years

  * First-time ischemic or hemorrhagic stroke
  * Subacute stroke (\<6 months)
  * Brunnstrom stage ≥ 3 (lower limb)
  * Able to walk 10 meters independently or with minimal support
  * Able to follow simple commands

Exclusion Criteria:

* • Severe aphasia

  * Other neurological disorders (Parkinson's, TBI)
  * Uncontrolled cardiovascular issues (BP \> 180 mmHg, arrhythmias)
  * Severe visual, auditory, or orthopedic impairments
  * Musculoskeletal injuries or medical conditions limiting participation
  * Diabetes, hypertension, fractures, surgeries, OA, RA

Where it's running

  • Civil Hospital Daska, Pakistan
    Daska Kalan, Pakistan
    Recruiting

Study contacts

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.