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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02614677
Other study ID # CCH-140713
Secondary ID
Status Completed
Phase N/A
First received November 8, 2015
Last updated November 22, 2015
Start date August 2014
Est. completion date December 2014

Study information

Verified date November 2015
Source Changhua Christian Hospital
Contact n/a
Is FDA regulated No
Health authority Taiwan: Institutional Review Board
Study type Observational

Clinical Trial Summary

Before 2007, the disability evaluation was based on the medical model in Taiwan. According to the People with Disabilities Rights Protection Act announced on 11 July 2007, the assessment of a person's eligibility for disability benefits has to be determined as suffering one of eight malfunction categories based on the International Classification of Functioning, Disability, and Health (ICF) framework. People with disabilities want to issue a disability identification and other welfare & services need processes of evaluation & assessment based on the ICF framework for the evaluation report and result of living need by the committee composed of professionals from medicine, social work, special education and employment counseling and evaluation.

In this year, investigators planed the project with the Taiwan Society of ICF to develop the evaluation form. The experts from various disciplines of the ICF Office convened internal integration meetings to reach a consensus for developed the ICF evaluation form, add the code of pain and sleep and the items from Short-Form 12 for quality of life to the questionnaire. The results were used to analysis other relevant factors affecting the disability evaluation. And then add the core set from World Health Organization to both physical and mental disorders linked coding group, compared the new disability evaluation system and evaluate the living need of people with disability to provide suggestion for core set.


Recruitment information / eligibility

Status Completed
Enrollment 250
Est. completion date December 2014
Est. primary completion date December 2014
Accepts healthy volunteers No
Gender Both
Age group 6 Years to 65 Years
Eligibility Inclusion Criteria:

- comply with a standard of the disability evaluation

Exclusion Criteria:

Study Design

Observational Model: Case-Only, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
Taiwan Changhua Christian Hospital Taiwan Changhua

Sponsors (1)

Lead Sponsor Collaborator
Changhua Christian Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Assessment of Quality of life by disability evaluate system One day when patients came first Yes
Primary Pain intensity on the Numerical Rating Scale One day when patients came first Yes
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