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Enhancing Post-Stroke Dysphagia Rehabilitation (Not exist)

Hamad Medical Corporation (HMC) logo

Hamad Medical Corporation (HMC)

Status

Enrolling

Conditions

Dysphagia After Stroke

Treatments

Procedure: Swallowing exercise (Expiratory Muscle Strength Training)
Procedure: Neuromuscular Electrical Stimulation
Procedure: Neuromuscular Taping
Procedure: Swallowing exercise (Chin Tuck Against Resistance)

Study type

Interventional

Funder types

Industry

Identifiers

NCT06887855
Not exist (Other Grant/Funding Number)
MRC-01-23-242

Details and patient eligibility

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.

Full description

This proposed study will be conducted using a prospective, three-group, randomized controlled trial. The participants for this study will be recruited from the post-acute and rehabilitation units who are diagnosed with post-stroke dysphagia at Hamad Medical Corporation hospitals in the State of Qatar.

Enrollment

10 estimated patients

Sex

All

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 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.

Exclusion criteria

  • Post-stroke patients with severe cognitive impairment,
  • Patients who have swallowing disorders due to other etiologies,
  • Patients who need traditional swallowing therapy other than Expiratory Muscle Strength Training (EMST) and Chin Tuck Against Resistance (CTAR). - Skin disorders in the submental area and anterior neck,
  • Medical conditions that may affect participation,
  • A defibrillator and use precision electrical biomedical devices (e.g. pacemaker, etc.).

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

10 participants in 3 patient groups

Group A
Experimental group
Description:
Participants will receive neuromuscular electrical stimulation + swallowing exercises ( chin tuck against resistance + expiratory muscle strength training)
Treatment:
Procedure: Swallowing exercise (Chin Tuck Against Resistance)
Procedure: Neuromuscular Electrical Stimulation
Procedure: Swallowing exercise (Expiratory Muscle Strength Training)
Group B
Experimental group
Description:
Participants will receive neuromuscular taping + swallowing exercises (chin tuck against resistance + expiratory muscle strength training)
Treatment:
Procedure: Swallowing exercise (Chin Tuck Against Resistance)
Procedure: Neuromuscular Taping
Procedure: Swallowing exercise (Expiratory Muscle Strength Training)
Group C
Experimental group
Description:
Participants will receive neuromuscular electrical stimulation + neuromuscular taping + swallowing exercises (chin tuck against resistance + expiratory muscle strength training)
Treatment:
Procedure: Swallowing exercise (Chin Tuck Against Resistance)
Procedure: Neuromuscular Taping
Procedure: Neuromuscular Electrical Stimulation
Procedure: Swallowing exercise (Expiratory Muscle Strength Training)

Trial contacts and locations

1

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Central trial contact

Ibrahim Mohammad Alayaseh, M. Sc. _ SLP

Data sourced from clinicaltrials.gov

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