Development of a Comprehensive ADL Scale for Stroke Patients
Recruitment status was Recruiting
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Purpose
our research team will develop a new CADL scale for stroke patients over the next three years.
In the first year, we had established a CADL item bank of 50 items. The investigators will administer the 50 items on 300 patients with stroke living in the community. Then we will select 10 to 15 items from the item bank for the CADL scale based on the International Classification of Functioning, Disability and Health (ICF), the opinions of an expert panel, and Rasch analysis. It is anticipated that the CADL scale will have unidimensionality, an interval level of measurement, soundly psychometric characteristics, a reduced number of items, and ease of administration.
In the second and third years, we will compare the psychometric properties of the CADL scale and the combined BI and FAI scale. The psychometric properties investigated will include reliability (e.g. inter-rater reliability, intra-rater reliability, and internal consistency), validity (e.g. concurrent validity, convergent validity, predictive validity and discriminant validity), and responsiveness. A total of 150 patients will be recruited. Both the CADL scale and the combined BI and FAI scale will be used on patients from the initial stage (within one month) to six months after hospital discharge. The results will be useful for researchers and clinicians to determine whether the CADL scale is better than the combined BI and FAI scale in stroke patients.
| Condition |
|---|
|
Cerebrovascular Accidents |
| Study Type: | Observational |
| Study Design: | Additional Descriptors: Psychosocial Observational Model: Defined Population Time Perspective: Longitudinal Time Perspective: Prospective |
| Official Title: | Development of a Comprehensive ADL Scale for Stroke Patients |
| Estimated Enrollment: | 300 |
| Study Start Date: | August 2004 |
| Estimated Study Completion Date: | May 2007 |
our research team will develop a new CADL scale for stroke patients over the next three years.
In the first year (an ongoing project: NSC 93-2314-B-002-284), we had established a CADL item bank of 50 items. The investigators will administer the 50 items on 300 patients with stroke living in the community. Then we will select 10 to 15 items from the item bank for the CADL scale based on the International Classification of Functioning, Disability and Health (ICF), the opinions of an expert panel, and Rasch analysis. It is anticipated that the CADL scale will have unidimensionality, an interval level of measurement, soundly psychometric characteristics, a reduced number of items, and ease of administration.
In the second and third years, we will compare the psychometric properties of the CADL scale and the combined BI and FAI scale. The psychometric properties investigated will include reliability (e.g. inter-rater reliability, intra-rater reliability, and internal consistency), validity (e.g. concurrent validity, convergent validity, predictive validity and discriminant validity), and responsiveness. A total of 150 patients will be recruited. Both the CADL scale and the combined BI and FAI scale will be used on patients from the initial stage (within one month) to six months after hospital discharge. The results will be useful for researchers and clinicians to determine whether the CADL scale is better than the combined BI and FAI scale in stroke patients.
Eligibility| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
diagnosis of stroke
Exclusion Criteria:
with other major diseases (e.g., cancer)
Contacts and Locations| Contact: I-Ping Hsueh, MA | 886-23123456 ext 7568 | iping@ha.mc.ntu.edu.tw |
| Taiwan | |
| School of Occupational Therapy, College of Medicine, National Taiwan University | Recruiting |
| Taiwan, Taiwan, 100 | |
| Contact: I-Ping Hsueh, MA 886-23123456 ext 7568 iping@ha.mc.ntu.edu.tw | |
| Principal Investigator: I-Ping Hsueh, MA | |
| Principal Investigator: | I-Ping Hsueh, MA | School of Occupational Therapy, College of Medicine, National Taiwan University |
More Information
No publications provided
| ClinicalTrials.gov Identifier: | NCT00173771 History of Changes |
| Other Study ID Numbers: | 9361701233, NSC-94-2314-B-002-076 |
| Study First Received: | September 13, 2005 |
| Last Updated: | September 13, 2005 |
| Health Authority: | Taiwan: Department of Health |
Keywords provided by National Taiwan University Hospital:
|
stroke activities of daily living psychometrics |
Additional relevant MeSH terms:
|
Cerebral Infarction Stroke Brain Infarction Brain Ischemia Cerebrovascular Disorders |
Brain Diseases Central Nervous System Diseases Nervous System Diseases Vascular Diseases Cardiovascular Diseases |
ClinicalTrials.gov processed this record on June 18, 2013