CClinicalTrials.gg
CompletedNCT06174025Updated Jan 12, 2024

Validity and Reliability of the 6 Minute Pegboard Ring Test

An observational study in Duchenne Muscular Dystrophy, sponsored by Çağtay Maden. Completed at 1 site in Turkey. Open to male participants aged 6 Years to 18 Years. Per ClinicalTrials.gov, last updated 2024-01-12.

Sponsored by Çağtay Maden · Observational

Study type
Observational
Model
Case-only
Time perspective
Cross-sectional
Enrollment
22
Ages
6 Years to 18 Years
Sex
Male
01

Study summary

This study aimed to investigate the validity and reliability of 6PBRT in individuals with DMD and its applicability on these patients.

Read the detailed description

Duchenne muscular dystrophy (DMD) is the most common type of progressive muscular dystrophies and is an X-linked recessive, rarely autosomal dominant, muscle disease. DMD begins in childhood and progresses until they become unable to walk. Individuals with DMD experience skeletal muscle weakness, difficulty breathing, and decreased exercise capacity. In these patients, traditionally lower extremity tests are; 6-minute walk tests, treadmill tests and Cardiopulmonary exercise tests are used. However, it is reported that the upper extremity is also affected in individuals with DMD. The 6-Minute Pegboard and Ring Test (6PBRT), which is valid and reliable in most disease groups, is also a test that can be applied to the upper extremities. It is important to use 6PBRT frequently in clinical research practice for patients with DMD and to know its validity and reliability. To our knowledge, the validity and reliability of this test in individuals with DMD has not been established in the literature. This study aimed to investigate the validity and reliability of 6PBRT in individuals with DMD and its applicability on these patients.

02

Conditions studied

  • Duchenne Muscular Dystrophy

Keywords

  • Duchenne Muscular Dystrophy
  • 6 Minute Pegboard and Ring Test
  • arm exercise endurance
  • upper extremity
03

In context

Muscular Dystrophies

548 studies on the registry are indexed under Muscular Dystrophies; 89 are open to participants now.

This study's enrollment of 22 is below the median of 69 across 179 observational studies indexed under Muscular Dystrophies.

Browse Muscular Dystrophies studies →

Lead sponsor

Çağtay Maden is the lead sponsor of 2 studies on the registry; none are open to participants now.

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

04

Who can participate

Ages eligible
6 Years to 18 Years
Sexes eligible
Male
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Individuals diagnosed with Duchenne muscular dystrophy

Inclusion criteria

  • Volunteering to participate in the research,
  • Being diagnosed with Duchenne muscular dystrophy between the ages of 6-17,
  • Being Level 1 and 2 according to the Brooke Upper Extremity Functional Classification Scale
  • Having no problems reading and/or understanding the scales and cooperating with the tests to be.
  • Ability to sit independently for approximately 15 minutes during the evaluation

Exclusion criteria

Exclusion Criteria:

  • Not volunteering to participate in the research,
  • Having any orthopedic problem in the upper extremity,
  • A neurological disease or other clinical condition that may affect cognitive status having a diagnosis,
  • Having had surgery on the upper extremities in the last 6 months and any having an injury
  • At a level that prevents functional activities in the upper extremity Having severe contractures (joint restriction)
05

Study design

Observational model
Case-only
Time perspective
Cross-sectional
Enrollment
22 participants (actual)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. 6 Minute Pegboard and Ring Test

    The 6-minute pegboard and ring test is used to assess upper extremity functional capacity. The patient sat in front of a perforated board with bottom pegs at shoulder level. The upper pegs are placed in the hole 20 cm above the lower pegs. 10 rings of the same size are placed on the lower pegs. The patient is asked to move as many rings as possible from the lower pegs to the upper pegs and vice versa within a 6-minute period. Pulse, blood pressure, SpO₂, dyspnea and arm fatigue detection are recorded before/after each test. Before the actual test, patients are allowed to move up and down the rings in a cycle to become familiar with the testing procedure. If the patient wants to rest during the test, he is allowed, but the stopwatch is not stopped. During the test, standard encouraging phrases are said to the patient at the end of each minute.

    Time frame: A total of two measurements will be made at 1-week intervals within 6 months.

Secondary outcomes

  1. Quick Shoulder-Hand Syndromes Questionnaire

    The Quick Shoulder-Hand Syndromes Questionnaire is used to evaluate musculoskeletal physical function and symptoms of the upper extremity. The survey consists of 11 items and is scored between 0-100 points. Higher scores indicate more disability

    Time frame: A total of two measurements will be made at 1-week intervals within 6 months.

  2. Assessment of muscle strength

    Muscle strength will be measured using a digital dynamometer (Manual Muscle Tester™), shoulder flexor, shoulder abductor, elbow extensor and elbow flexor muscle strength. Muscle tests will be repeated three times for each side and the highest value will be recorded in kg. Muscle strength will be calculated as percentages of expected values.

    Time frame: A total of two measurements will be made at 1-week intervals within 6 months.

  3. The Pediatric Quality of Life Inventory

    The health-related quality of life of the participants will be evaluated with the Turkish version PedsQL-3.0 Neuromuscular Module. The scale consists of 3 categories containing 25 items. These categories; It includes 17 items regarding the disease process and related symptoms, 3 items regarding communication skills, and 5 items regarding the family's financial and social support systems. The items of the scale are scored between 4 (always poses a problem) and 0 (never poses a problem). At the end of the scale, a score between 0 and 4 is made. A score close to 100 indicates that the health-related quality of life is at a better level.

    Time frame: A total of two measurements will be made at 1-week intervals within 6 months.

  4. Brooke Upper Extremity Functional Classification Scale

    It will be used to evaluate the upper extremity functional level of the individuals who will be included in the study. It was developed to determine the functional level of the upper extremity in the clinical evaluation of DMD (11). The steps of this scale are as follows; Level 1: Begins to move with the arms at the sides and can fully clasp the hands above the head. Level 2: However, he can bring his arms above his head by flexing his elbows or use his accessory muscles Level 3: He cannot raise his hands above his head, but he can bring the glass to his mouth (uses both hands if necessary). Level 4: He can raise his hands to his mouth, but cannot lift a glass of water to his mouth. Level 5: Cannot raise hands to mouth, but can raise hands to hold a pen or pick up a coin from the table. Level 6: He cannot raise his hands up to his mouth and cannot use his hands functionally.

    Time frame: A total of two measurements will be made at 1-week intervals within 6 months.

07

Study locations

1 site
  • Gaziantep İslamic Science and Technology University
    Gaziantep, Şahinbey 27000, Turkey
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 12, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06174025
Lead sponsor
Çağtay Maden
Responsible party
Çağtay Maden (Assistant professor, Gaziantep Islam Science and Technology University) — Sponsor-investigator
First posted
Dec 18, 2023
Start date
Jun 30, 2023
Primary completion
Dec 30, 2023
Completion
Jan 1, 2024
Last update
Jan 12, 2024

Study contacts

Çağtay MADEN, PhD
principal investigator · Gaziantep İslamic Science and Technology University

Oversight

Data monitoring committee
No
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 May 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