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

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

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07724730
Enrollment
38
Registered
2026-07-24
Start date
2025-06-01
Completion date
2026-08-05
Last updated
2026-07-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stroke

Keywords

Rhythmic Auditory Stimulation, Task-Oriented Training, Balance, Proprioception, Lower Extremity Function, Motivation, Rehabilitation Adherence

Brief summary

Stroke is one of the leading causes of long-term disability worldwide. Among survivors, limitations in lower limb motor function, balance, and proprioception significantly affect their independence and quality of life. There is a growing need for targeted rehabilitation strategies for stroke survivors, who often experience lower limb impairments that limit independence during a highly active stage of life. Task-oriented training (TOT) helps patients practice real-life movements, while rhythmic auditory stimulation (RAS), such as metronome beats, can guide and improve their timing and coordination.

Detailed description

It will be a single blinded randomized controlled trial. Non-probability convenience sampling technique will be used to recruit 38 participants aged 40 to 60 years, subacute stage post-stroke from hospitals of Daska and NLH Physio Clinic. Sealed opaque method will be used to randomly divide into two groups. Group A will receive TOT along with RAS, while Group B will receive only TOT. Both groups will participate in supervised 30-minute exercise sessions, including a 10-minute warm-up and cool-down period, five days a week for eight weeks, in addition to 30 minutes of baseline conventional physiotherapy program. The interventions will focus on lower limb function, balance, proprioceptive training, and motivational engagement. Tools used for outcome assessment include the Lower Extremity Functional Scale (LEFS) for motor function, Timed Up and Go (TUG) test for dynamic balance, Joint Position Sense (JPS) test for proprioception, Stroke Rehabilitation Motivation Scale (SRMS) for motivation, and the Rehabilitation Adherence Questionnaire (RAQ) for adherence. Data will be analyzed using SPSS version 25 to compare pre- and post-intervention effects. . After assessing the normality, if the p-value is greater than 0.05, a parametric test will be applied. If the p-value is less than 0.05 then a non-parametric test will be applied.

Interventions

OTHERTask-Oriented Training + Rhythmic Auditory Stimulation

* 30-minute TOT session + RAS (60-110 BPM progression) * Functional gait tasks, obstacle walking, stair climbing, balance tasks * 5 days/week for 8 weeks * Plus 30-minute baseline physiotherapy

* Same TOT structure without rhythmic cues * Functional lower limb tasks, balance training, gait practice * 5 days/week for 8 weeks * Plus 30-minute baseline physiotherapy

Sponsors

Riphah International University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Masking description

An independent assessor, who is blinded to the group allocations, will be responsible for evaluating study outcomes.

Intervention model description

Randomized Clinical Trial

Eligibility

Sex/Gender
ALL
Age
40 Years to 60 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Lower Limb Motor FunctionBaseline and Week 8Lower Extremity Function (LEFS)
Dynamic BalanceBaseline and Week 8Time up and Go Test
ProprioceptionBaseline and post 8 weeksJoint Position Sense Test
motivationBaseline and post 8 weeksStroke Rehabilitation Motivation Scale (SRMS)
adherenceBaseline and post 8 weeksRehabilitation Adherence Questionnaire (RAQ)

Countries

Pakistan

Contacts

CONTACTImran Amjad, PhD
imran.amjad@riphah.edu.pk03324390125
PRINCIPAL_INVESTIGATORAiza Yousaf, MS-OMPT

Riphah International University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 25, 2026