Investigating Program of Food Preparation on Diet Improvement for Patients With Stroke

NCT ID: NCT04347863

Last Updated: 2020-04-15

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

22 participants

Study Classification

INTERVENTIONAL

Study Start Date

2018-04-19

Study Completion Date

2018-09-28

Brief Summary

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This is a randomized controlled behavioral intervention trial to assess the efficacy of investigating program of food preparation on diet improve patients with stroke.

Detailed Description

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This is a randomized controlled behavioral intervention trial to assess the efficacy of investigating program of food preparation on diet improve patients with stroke. Subjects will be randomized to intervention group and control group.The primary outcome included seven measures, Functional oral intake scale, Mini Nutritional Assessment, Council on Nutrition Appetite Questionnaire, Dietary Well-Being Scale, Swallowing Quality of Life questionnaire, WHO Quality of Life-BREF and Eating Assessment Tool-10.

Conditions

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Stroke Dysphagia, Late Effect of Stroke

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

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Experimental group

Group swallowing disorder diet preparation program

Group Type EXPERIMENTAL

Group swallowing disorder diet preparation program

Intervention Type OTHER

This program included food properties, select food, type of cooking, using thickener and tasting

Control group

No Intervention

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Group swallowing disorder diet preparation program

This program included food properties, select food, type of cooking, using thickener and tasting

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Diagnosis is stroke
* EAT-10 ≥ 3
* Aged \> 20 years
* Capability of following instructions
* Willing to participants to the study

Exclusion Criteria

* Non-stroke neurological diseases ( ex: traumatic brain injury, brain tumor, neurodegenerative disease and Parkinson's disease )
* Dysphagia by neck injury or surgery
* During the study, he/she was hospitalized again due to disease.
Minimum Eligible Age

20 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Taiwan Adventist Hospital

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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En-Chi Chiu, PhD

Role: STUDY_DIRECTOR

National Taipei University of Nursing and Health Sciences

Locations

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National Taipei University of Nursing and Health Sciences

Taipei, Beitou Dist, Taiwan

Site Status

Countries

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Taiwan

Other Identifiers

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106-E-29

Identifier Type: -

Identifier Source: org_study_id

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