CClinicalTrials.gg
CompletedNCT05215795Updated Jan 13, 2023

Validity and Reliability of Modified Box and Block Test and Targeted Box and Block Test in Patients With Stroke

An observational study in Stroke, sponsored by Kutahya Health Sciences University. Completed at 1 site in Turkey. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2023-01-13.

Sponsored by Kutahya Health Sciences University · Observational

Study type
Observational
Model
Other
Time perspective
Prospective
Enrollment
50
Ages
18 Years and older
Sex
All
01

Study summary

The aim of our study is investigated validity and reliabilty of Modified Box and Block Test and Targeted Box and Block Test in patients with stroke.

Read the detailed description

Fifty patients with stroke will included in the study. Box and Block Test, Modified Box and Block Test, Targeted Box and Block Test, 9 Hole Peg Test, Fugl-Meyer Assessment of the upper extremity will used to assess upper extremity. To evaluate validity between Modified and Targeted Box and Block Tests and Box and Block Test, 9 Hole Peg Test, Fugl-Meyer Assessment will used to correlation analysis tests. The investigator will evaluate after one week to test-retest reliability to patients. Other pyhsiotherapist will evaluate to patients inter-rater reliability.

02

Conditions studied

  • Stroke

Browse trials for

Keywords

  • Validity
  • Reliability
  • Modified Box and Block Test
  • Targeted Box and Block Test
  • Upper Extremity
03

In context

Stroke

7,286 studies on the registry are indexed under Stroke; 2,007 are open to participants now.

This study's enrollment of 50 is below the median of 160 across 1,692 observational studies indexed under Stroke.

Browse Stroke studies →

Lead sponsor

Kutahya Health Sciences University is the lead sponsor of 209 studies on the registry; 46 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Patients with stroke

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

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
05

Study design

Observational model
Other
Time perspective
Prospective
Enrollment
50 participants (actual)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. Modified Box and Block Test

    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.

    Time frame: 10 minute

  2. Targeted Box and Block Test

    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.

    Time frame: 10 minute

Secondary outcomes

  1. 9 Hole Peg Test

    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.

    Time frame: 10 minute

  2. Fugl-Meyer Assessment for Upper Extremity

    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

    Time frame: 15 minutes

  3. Box and Block Test

    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.

    Time frame: 5 minute

07

Study locations

1 site
  • Kutahya Health Sciences University
    Kütahya, 43100, Turkey
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 13, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT05215795
Lead sponsor
Kutahya Health Sciences University
Responsible party
Lütfiye AKKURT, MSc (Lecturer, MSc PT, Kutahya Health Sciences University) — Principal investigator
First posted
Jan 31, 2022
Start date
Sep 1, 2021
Primary completion
Oct 1, 2022
Completion
Oct 1, 2022
Last update
Jan 13, 2023

Study contacts

Lütfiye AKKURT, MSc
principal investigator · Kutahya Health Sciences University
Cihan Caner AKSOY, PhD
study director · Kutahya Health Sciences University
Fatıma YAMAN, MD
principal investigator · Kutahya Health Sciences University

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jan 2023. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion