Cerebrovascular AccidentsNCT00173810
Development of a Refined Version of the Stroke Rehabilitation Assessment of Movement Scale for Stroke Patients
An observational study of Cerebrovascular Accidents, run by National Taiwan University Hospital at 1 site in Taiwan.
Trial summary
We will employ modern test theory (i.e., Rasch model) to refine the Stroke Rehabilitation Assessment of Movement instrument (STREAM), which will be called the refined version of the STREAM, R-STREAM). Read more about this study
- Who is it for?
- Ages 0 years and older
- Conditions the study is for
- Cerebrovascular Accidents
- How many people
- 300 participants
- Where
- 1 siteTaiwan
- Study dates
- Aug 2005to Apr 2007
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 0 years and older
- All sexes
- No healthy volunteers
- Child, Adult, Older adult
Who may be able to join
- patients with stroke ability to follow instructions
Who cannot join
- patients with other major diseases (e.g., cancer)
Trial locations and contacts
1 site in 1 country.
Taiwan1 site, 1 recruiting
- Recruiting
School of Occupational Therapy, College of Medicine, National Taiwan University
Taipei, 100
I-Ping Hsueh, MA, 886-2-23123456 ext. 7568, iping@ha.mc.ntu.edu.tw
I-Ping Hsueh, MA
About this study
We will employ modern test theory (i.e., Rasch model) to refine the Stroke Rehabilitation Assessment of Movement instrument (STREAM), which will be called the refined version of the STREAM, R-STREAM).
Read the detailed description
We will employ modern test theory (i.e., Rasch model) to refine the Stroke Rehabilitation Assessment of Movement instrument (STREAM), which will be called the refined version of the STREAM, R-STREAM).
We will devote three years to complete this project. In the first year, the item pool (about 45 items) based on the STREAM will be developed and 12-15 items will be selected from the pool to construct the R-STREAM. A therapist will administer all the items on 300 stroke patients. The other therapist will administer these items on 60 patients randomly selected from the 300 patients to examine interrater reliability of each item. The R-SATREAM (4-5 items for each of the three subscales) will be constructed based on the inter-rater reliability and Rasch analysis of these items, and the opinions of experts.
In the second and third years of this project, the psychometric properties of the R-STREAM will be comprehensively established. We will also compare the psychometric properties of the R-STREAM and the STREAM in stroke patients to determine the psychometric properties and efficiency of the R-STREAM. The R-STREAM and STREAM will be used to longitudinally assess 120 patients (at three time points: at the conception of occupational therapy, one month after therapy, and 6 months after therapy) to compare the concurrent validity, predictive validity and responsiveness of the R-STREAM and STREAM. The test-retest reliability of both scales will be established on the other 60 chronic patients.
It is anticipated that the R-STREAM will have sound psychometric properties, be simple and easy to use, and be able to be transformed to the interval level of measurement. The R-STREAM will best fit the need for simple measures in routine daily clinics. The R-STREAM will fit demands for both in-depth and efficient assessment. Clinicians and researchers both will benefit from these new, scientific measurement tools for planning treatment, giving a prognosis, and assessing outcomes in stroke patients.
- Conditions
- Cerebrovascular Accidents
- Keywords
- stroke, movement, psychomterics
- Medical subject headings
- Stroke
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted15 Sep 2005 (estimated)
- Study startAug 2005
- Study completionApr 2007
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Cerebrovascular AccidentsStudies of the same condition, open and under way.
- More trials run by National Taiwan University HospitalThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Defined population
- Time perspective
- Prospective
- Enrolment
- 300 participants
Sponsor and investigators
- Lead sponsor
- National Taiwan University Hospital
- Sponsor type
- University, hospital or other
- Collaborators
- National Science and Technology Council, Taiwan
- Investigators
- I-Ping Hsueh, MA, Principal investigator, School of Occupational Therapy, College of Medicine, National Taiwan University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT00173810
- Sponsor's protocol ID
- 9361701234
- Other IDs
- NSC-94-2314-B-002-078
- Status last verified
- Jul 2005
- First submitted
- 13 Sep 2005
- Last updated
- 15 Sep 2005
- Results posted
- No
Study at a glance
From the registry record, last updated by the sponsor on 15 Sep 2005. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Development of a Refined Version of the Stroke Rehabilitation Assessment of Movement Scale for Stroke Patients
- ClinicalTrials.gov ID
- NCT00173810
- Acronym / sponsor ID
- 9361701234
- Conditions
- Cerebrovascular Accidents
- Keywords
- stroke, movement, psychomterics
- Study type
- Observational
- Recruitment status
- Unknown status
- Enrolment
- 300 participants
- Lead sponsor
- National Taiwan University HospitalUniversity, hospital or other
- Collaborators
- National Science and Technology Council, Taiwan
- Study start
- Aug 2005
- Study completion
- Apr 2007
- First posted
- 15 Sep 2005 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
We will employ modern test theory (i.e., Rasch model) to refine the Stroke Rehabilitation Assessment of Movement instrument (STREAM), which will be called the refined version of the STREAM, R-STREAM).
Detailed description
We will employ modern test theory (i.e., Rasch model) to refine the Stroke Rehabilitation Assessment of Movement instrument (STREAM), which will be called the refined version of the STREAM, R-STREAM).
We will devote three years to complete this project. In the first year, the item pool (about 45 items) based on the STREAM will be developed and 12-15 items will be selected from the pool to construct the R-STREAM. A therapist will administer all the items on 300 stroke patients. The other therapist will administer these items on 60 patients randomly selected from the 300 patients to examine interrater reliability of each item. The R-SATREAM (4-5 items for each of the three subscales) will be constructed based on the inter-rater reliability and Rasch analysis of these items, and the opinions of experts.
In the second and third years of this project, the psychometric properties of the R-STREAM will be comprehensively established. We will also compare the psychometric properties of the R-STREAM and the STREAM in stroke patients to determine the psychometric properties and efficiency of the R-STREAM. The R-STREAM and STREAM will be used to longitudinally assess 120 patients (at three time points: at the conception of occupational therapy, one month after therapy, and 6 months after therapy) to compare the concurrent validity, predictive validity and responsiveness of the R-STREAM and STREAM. The test-retest reliability of both scales will be established on the other 60 chronic patients.
It is anticipated that the R-STREAM will have sound psychometric properties, be simple and easy to use, and be able to be transformed to the interval level of measurement. The R-STREAM will best fit the need for simple measures in routine daily clinics. The R-STREAM will fit demands for both in-depth and efficient assessment. Clinicians and researchers both will benefit from these new, scientific measurement tools for planning treatment, giving a prognosis, and assessing outcomes in stroke patients.
Study design
- Observational model
- Defined population
- Time perspective
- Prospective
Who may qualify
- Ages
- 0 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult, Older adult
Key inclusion criteria (1 listed)
- patients with stroke ability to follow instructions
Key exclusion criteria (1 listed)
- patients with other major diseases (e.g., cancer)
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Not reported in the source record.
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 15 Sep 2005.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
I-Ping Hsueh, MA principal investigator
School of Occupational Therapy, College of Medicine, National Taiwan University
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Cerebrovascular Accidents, run by National Taiwan University Hospital at 1 site in Taiwan.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: status not confirmed, as of the sponsor's last update on 15 Sep 2005. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Taiwan. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Contact I-Ping Hsueh, MA (886-2-23123456 ext. 7568, iping@ha.mc.ntu.edu.tw), or a site near the patient. AzTrials does not enrol participants or take referrals.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 15 Sep 2005.