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Improving Breathing in Stroke Survivors: The Impact of Electrical Muscle Stimulation on Abdominal and Respiratory Muscles

Effect of neuromuscular electrical stimulation on rectus abdominus and transverse abdominus on the respiratory parameters in stroke survivors- a randomized controlled trial - NIL

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/05/067301
Enrollment
34
Registered
2024-05-14
Start date
Unknown
Completion date
Unknown
Last updated
2025-02-03

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

Conditions

Health Condition 1: G968- Other specified disorders of central nervous system

Interventions

Intervention1: Neuro-muscular electrical stimulator: Dosage of the neuro muscular electrical stimulation: frequency of 50Hz , pulse duration of 300 microseconds, rise time of 1 second
stimulus time of 3 seconds, and relaxation time of 10 seconds. Gradual increase in the intensity until significant muscle contraction occurs. Stimulation will be given for 20 minutes for 5 days. Contr

Sponsors

NITTE Institute of physiotherapy, NITTE (Deemed to be university)
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Consent of the patient to participate in the study is required. Participants should be aged between 40 and 75 years, inclusive of both men and women, with a clinical diagnosis of stroke. The patient must be hemodynamically stable on the day of examination and intervention. The duration of stroke from onset should be up to 6 months.

Exclusion criteria

Exclusion criteria: Patients with a history of seizures, individuals who have undergone thoracic or abdominal surgery in the past year, and those experiencing respiratory tract infections should be noted. Additionally, consideration should be given to patients with chronic respiratory diseases affecting respiratory muscle function (such as bronchial asthma or COPD), individuals with grade 4 and 5 strength of abdominal muscles, and patients with pacemakers.

Design outcomes

Primary

MeasureTime frame
Spirometry, palpation meter (PALM) device, chest expansion, Barthel IndexTimepoint: outcomes will be assessed at baseline and after 1 week of intervention

Secondary

MeasureTime frame
NILTimepoint: NIL

Countries

India

Contacts

Public ContactMr Jayesh Chandran

NITTE INSTITUTE OF PHYSIOTHERAPY, NITTE DEEMED TO BE UNIVERSITY

jayesh.nairpt@nitte.edu.in9383443710

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026