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The Impact of Diaphragm Training on Dysphagia in Bulbar Palsy After Ischemic Stroke

C

Copka Sonpashan

Status

Not yet enrolling

Conditions

Bulbar Palsy

Treatments

Behavioral: Routine rehabilitation
Behavioral: Diaphragm Training
Device: Intermittent Oro-esophageal Tube Feeding

Study type

Interventional

Funder types

Other

Identifiers

NCT06393218
GEJI-Zhenqiu

Details and patient eligibility

About

This was a prospective multicenter study. the patients after stroke with were randomly divided into the observation group and the control group. All patients were given comprehensive rehabilitation therapy. During the treatment, enteral nutrition support was provided for the two groups by Intermittent Oro-esophageal tube feeding. The observation group will be given Diaphragm Training Nutritional status, dysphagia, quality of life and depression before and after treatment were compared.

Full description

Dysphagia in patients after stroke continues to be a challenge. This was a prospective multicenter study. the patients after stroke with were randomly divided into the observation group and the control group. All patients were given comprehensive rehabilitation therapy. During the treatment, enteral nutrition support was provided for the two groups by Intermittent Oro-esophageal tube feeding. The observation group will be given Diaphragm Training Nutritional status, dysphagia, quality of life and depression before and after treatment were compared.

Enrollment

100 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • age ≥ 18 years;
  • meeting the diagnostic criteria of Bulbar Palsy After Ischemic Stroke;
  • any degree of dysphagia at admission;
  • steady vital signs, without severe cognitive impairment or sensory aphasia, able to cooperate with the assessment.
  • clear mind.

Exclusion criteria

  • complicated with other neurological diseases;
  • damaged mucosa or incomplete structure in nasopharynx;
  • tracheostomy tube plugged;
  • unfeasible to the support of parenteral nutrition;
  • simultaneously suffering from liver, kidney failure, tumors, or hematological diseases.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

100 participants in 2 patient groups

Routine rehabilitation+Diaphragm Training
Experimental group
Description:
Study lasts 15 days for each patient. The patients were given comprehensive rehabilitation therapy. The observation group was provided the support of enteral nutrition by Intermittent Oro-esophageal Tube Feeding. Diaphragm Training will be given twice a day and 30min per time.
Treatment:
Device: Intermittent Oro-esophageal Tube Feeding
Behavioral: Routine rehabilitation
Behavioral: Diaphragm Training
Routine rehabilitation
Active Comparator group
Description:
Study lasts 15 days for each patient. The patients were given comprehensive rehabilitation therapy. The observation group was provided the support of enteral nutrition by Intermittent Oro-esophageal Tube Feeding.
Treatment:
Device: Intermittent Oro-esophageal Tube Feeding
Behavioral: Routine rehabilitation

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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