Actively Recruiting

Phase Not Applicable
Age: 18Years - 75Years
All Genders
NCT06887855

Enhancing Post-Stroke Dysphagia Rehabilitation

Led by Hamad Medical Corporation · Updated on 2025-03-20

10

Participants Needed

1

Research Sites

60 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The goal of this clinical trial is to investigate the effects of a combined swallowing intervention (Neuromuscular Electrical Stimulation (NMES) + Neuromuscular Taping (NMT) + swallowing exercises) on swallowing function and quality of life in post-stroke dysphagia patients. The main questions it aims to answer are: • Does the combination of swallowing exercises, NMES \& NMT have a greater improvement in dysphagia rehabilitation when compared to either NMES or NMT alone? Researchers will compare the effects of intervention between the three groups (NMES and swallowing exercises, NMT and swallowing exercises, and NMES with NMT and swallowing exercises). Participants will: * Receive a combined dysphagia rehabilitation comprised of swallowing exercises, Neuromuscular Electrical stimulation, and/or Neuromuscular Taping. * Visit the clinic once every 5 days a week for 10 therapy sessions. * Undergo baseline and post-intervention evaluation procedures.

CONDITIONS

Official Title

Enhancing Post-Stroke Dysphagia Rehabilitation

Who Can Participate

Age: 18Years - 75Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients aged 18 - 75 years old
  • Diagnosed with swallowing disorders between one day and six months post-stroke
  • Able to attend 10 therapy sessions
  • Have never received any swallowing treatment before participating in this study
Not Eligible

You will not qualify if you...

  • Post-stroke patients with severe cognitive impairment
  • Patients who have swallowing disorders due to other causes
  • Patients requiring traditional swallowing therapy other than Expiratory Muscle Strength Training and Chin Tuck Against Resistance
  • Skin disorders in the submental area and anterior neck
  • Medical conditions that may affect participation
  • Presence of defibrillator or use of precision electrical biomedical devices such as pacemakers

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 1 location

1

Hamad Medical Corporation

Doha, Baladiyat ad Dawhah, Qatar, 3050

Actively Recruiting

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Research Team

I

Ibrahim Mohammad Alayaseh, M. Sc. _ SLP

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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