- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05215795
Validity and Reliability of Modified Box and Block Test and Targeted Box and Block Test in Patients With Stroke
Study Overview
Status
Conditions
Detailed Description
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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-
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Kütahya, Turkey, 43100
- Kütahya Health Sciences University
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Diagnosed with stroke and in the chronic phase (having been diagnosed with stroke at least 6 months ago),
- Over 18 years old,
- Mini Mental Test score ≥ 24 points,
- Able to grasp and release a 2.5 cm cube on both upper extremities,
- Brunnstrom Upper Extremity Staging ≥ 3
- Modified Ashworth Scale ≤ 2,
- Able to sit independently in a chair for 2 minutes
Exclusion Criteria:
- Having a neurological disease other than stroke
- Have had surgery in the last 6 months
- Severely affected upper extremity
- Uncooperative with physiotherapist
- Patients with neglect, aphasia and hemianopsia
Study Plan
How is the study designed?
Design Details
- Observational Models: Other
- Time Perspectives: Prospective
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Modified Box and Block Test
Time Frame: 10 minute
|
The Modified Box and Block (mBBT) test is an upper extremity performance test.Unlike BBT, in mBBT, instead of randomly picking the cubes, 16 cubes are arranged in a certain order. The cubes are asked to take the other cubes in that row, starting from the innermost left cube, first to the right, and then to the next upper row. It is recorded how many seconds passed through 16 cubes placed at a certain level. |
10 minute
|
Targeted Box and Block Test
Time Frame: 10 minute
|
In tBBT, as in mBBT, the time of passing 16 cubes over the obstacle to the other side is recorded. However, the difference from mKBT is that 16 cubes are placed at a certain level, but the patients are asked to place the cubes on the other side in 4 cm squares where the cube will be placed. These squares correspond to the left symmetrical position of the cube on the right. In this way, patients have to place the cube they grasp only at the desired point. |
10 minute
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
9 Hole Peg Test
Time Frame: 10 minute
|
9HPT is a dexterity test.The patient is asked to place the 9 wooden blocks into the 9 holes in the maximum amount of time.Then he is asked to take it out and put it back in its place.
The total time is recorded.
|
10 minute
|
Fugl-Meyer Assessment for Upper Extremity
Time Frame: 15 minutes
|
The Fugl-Meyer Assessment is a disease-specific impairment index designed to assess motor function, balance, sensation qualities and joint function in hemiplegic post-stroke patients.The scale consists of four categories (Shoulder/Elbow/Forearm, Wrist, Hand/Finger, and Coordination) and evaluates 23 different movements in 33 sections.The maximum score is 66 points
|
15 minutes
|
Box and Block Test
Time Frame: 5 minute
|
Box and Block (mBBT) test is an upper extremity performance test.
The patient is instructed to move as many blocks as possible, one at a time, from one compartment to the other for a period of 60 seconds.
The number of cubes passed to the other side in 60 seconds is recorded.
|
5 minute
|
Collaborators and Investigators
Investigators
- Principal Investigator: Fatıma YAMAN, MD, Kütahya Health Sciences University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- KutahyaHSU3
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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