Effect of Transcranial Direct Current Stimulation Combined With Oral Feeding on Dysphagia: A Randomized Controlled Study

Status: Recruiting
Location: See location...
Intervention Type: Device, Behavioral
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The study is a double-blind randomized controlled trial, lasting for 15 days for each participant. Patients with post-stroke dysphagia who receive treatment at the Rehabilitation Department are selected as the study subjects. The patients are randomly assigned to either the experimental group or the placebo group. All patients receive routine rehabilitation therapy and swallowing rehabilitation training, along with enteral nutrition support using Intermittent Oro-esophageal Tube. In addition to these interventions, patients in the experimental group receive transcranial direct current stimulation, while the instruments used for patients in the placebo group only illuminate an indicator light without any actual effect.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Meet the diagnostic criteria for ischemic stroke;

• Age \> 18 years;

• First-time stroke;

• Swallowing disorder confirmed by swallowing contrast study or flexible endoscopic evaluation of swallowing;

• Requires enteral nutrition support;

• Stable vital signs, no severe cognitive impairment or aphasia, able to cooperate with treatment;

• Transferred to the rehabilitation department within fifteen days of onset; Stable vital signs.

Locations
Other Locations
Taiwan
Hsinchu Rehabilitation Hospital
RECRUITING
Xinzhu
Contact Information
Primary
Zhefeng Wang, Master
zenghongjiclv@foxmail.com
19501376864
Backup
Weijia Li, Master
zwjww2009@163.com
13592505584
Time Frame
Start Date: 2024-02-28
Estimated Completion Date: 2024-05
Participants
Target number of participants: 80
Treatments
Experimental: The experimental group
The patients are randomly assigned to either the experimental group or the placebo group. All patients receive routine rehabilitation therapy and swallowing rehabilitation training, along with enteral nutrition support using Intermittent Oro-esophageal Tube. In addition to these interventions, patients in the experimental group receive transcranial direct current stimulation, while the instruments used for patients in the placebo group only illuminate an indicator light without any actual effect.
Placebo_comparator: The placebo group
The patients are randomly assigned to either the experimental group or the placebo group. All patients receive routine rehabilitation therapy and swallowing rehabilitation training, along with enteral nutrition support using Intermittent Oro-esophageal Tube. In addition to these interventions, patients in the experimental group receive transcranial direct current stimulation, while the instruments used for patients in the placebo group only illuminate an indicator light without any actual effect.
Related Therapeutic Areas
Sponsors
Leads: Zeng Changhao

This content was sourced from clinicaltrials.gov