- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02181036
Effects of Work Shop for Children With Developmental Delays
July 2, 2014 updated by: Taipei Medical University
Effects of Family Work Shop for Children With Speech Developmental Delays
To identify the effects of family work shop for children with speech developmental delays.
Study Overview
Detailed Description
To assess the improvement of functional performance of children with speech developmental delays by 2-3 hours per session, one session per week, a total of 6 weeks of family work shop
Study Type
Interventional
Enrollment (Anticipated)
30
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Taipei, Taiwan, 111
- Shin Kong Wu Ho-Su Memorial Hospital
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-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
1 year to 3 years (Child)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- 18 M/O to 36 M/O of children with speech development delay
Exclusion Criteria:
- less than 18 M/O older than 36 M/O
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: family work shop
2 to 3 hours per session, one session per week, for a total of 6 weeks of family work shop
|
2-3 hours per session, one session per week, a total of 6 weeks of family work shop
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
changes of pediatric health related quality of life (Pediatric Quality of Life Inventory)
Time Frame: participants will be evaluated at before and after 6 weeks of work shop
|
participants receive one 2-hour session of work shop per week for a 6-week duration
|
participants will be evaluated at before and after 6 weeks of work shop
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Director: Ru-Lan Hsieh, MD, Taipei Medical University
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
June 1, 2014
Primary Completion (Anticipated)
January 1, 2015
Study Completion (Anticipated)
January 1, 2015
Study Registration Dates
First Submitted
June 30, 2014
First Submitted That Met QC Criteria
July 2, 2014
First Posted (Estimate)
July 3, 2014
Study Record Updates
Last Update Posted (Estimate)
July 3, 2014
Last Update Submitted That Met QC Criteria
July 2, 2014
Last Verified
June 1, 2014
More Information
Terms related to this study
Other Study ID Numbers
- DOH-SKH-103-07
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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