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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT01967212
Other study ID # 201210059RIC
Secondary ID
Status Active, not recruiting
Phase N/A
First received October 13, 2013
Last updated October 17, 2013
Start date December 2012

Study information

Verified date October 2013
Source National Taiwan University Hospital
Contact n/a
Is FDA regulated No
Health authority Taiwan: Department of Health
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine whether swallowing training combined with game-based biofeedback is effective in the treatment of dysphagia due to stroke.


Description:

Swallowing maneuvers are very effective if done correctly, but to evaluate the use of force and the extent of laryngeal elevation is very difficult.

The therapist often requests the patient to "swallow hard" or "maintain laryngeal elevation". However, it is difficult to provide appropriate feedback to the patient, because it's hard to see the throat muscle contraction and bone displacement,the real point of the force is not clear, only oral and tactile feedback is inadequate and when combined with sensory loss, fatigue or cognition impairment.

Biofeedback is defined as "the technique of using equipment (usually electronic) to reveal internal physiological events by visual and auditory signals, to teach patients to manipulate the intrinsic physiological activity (Basmajian, 1989).The rationale is thus that if a patient sees his muscle activity, rather than just feels his muscles contract, he will be able to contract his muscles more fiercely and therefore he will be able to train his muscles faster.

Past studies have shown that biofeedback can help nerve injury patients control their physiological activities such as swallowing training.

The purpose of this study is to determine whether swallowing training combined with game-based biofeedback is effective in the treatment of dysphagia due to stroke.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 30
Est. completion date
Est. primary completion date December 2013
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 90 Years
Eligibility Inclusion Criteria:

- stroke

- above 18 years-old

- pharyngeal stage dysphagia

Exclusion Criteria:

- on trachea

- cannot follow one command

Study Design

Allocation: Non-Randomized, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Device:
Game-based swallow biofeedback
The intervention are divided into two parts: Traditional swallowing training 30 min by speech therapist. Game-based biofeedback combined with Mendelsohn's maneuver and effortful swallow 30 min by investigator.
Behavioral:
Swallow training without biofeedback
The intervention are divided into two parts: Traditional swallowing training 30 min by speech therapist. Mendelsohn's maneuver and effortful swallow without biofeedback 30 min.

Locations

Country Name City State
Taiwan National Taiwan University Hospital Taipei

Sponsors (1)

Lead Sponsor Collaborator
National Taiwan University Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Other SWAL-QOL Questionnaire 6-8 weeks Yes
Primary Hyoid bone displacement on the ultrasound 6-8 weeks Yes
Secondary Swallow functional ability on the Functional Oral Intake Scale 6-8 weeks Yes
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