The purpose of this study was to evaluate the validity and reliability of six-minute peg board and ring test (6-PBRT) in individuals with chronic neck pain and to determine the applicability of the test for this patient population.
Neck pain is the fourth leading cause of disability worldwide and is a significant public health problem. Chronic neck pain is defined as the presence of pain in the neck region of individuals for more than twelve weeks. Chronic neck pain is a disorder that negatively affects the individual's daily life activities and causes labor force and economic losses by causing functional limitations, loss of work and disability. It is important to evaluate the physical fitness components in detail in individuals with chronic neck pain. It has been stated that neck pain reduces upper extremity performance. Different measurement methods have been used to evaluate the upper extremity functions of individuals. Standard measurement tools are needed to evaluate the upper extremity exercise capacity in patients with chronic neck pain. The 6-PBRT is a valid, reliable, useful, practical and easy-to-apply test that evaluates the endurance of the upper extremity without support in healthy individuals and those with chronic obstructive pulmonary disease. The validity and reliability of 6-PBRT, which is used to evaluate functional upper extremity exercise capacity in different diseases, has not been investigated in individuals with chronic neck pain. The aim of this study was to evaluate the validity and reliability of 6-PBRT in individuals with chronic neck pain and to determine the applicability of the test for this patient population.
Study Type
OBSERVATIONAL
Enrollment
49
Kırşehir Ahi Evran University, 63 / 5.000 Physical Therapy and Rehabilitation Center, Cardiopulmonary Unit
Kırşehir, Center, Turkey (Türkiye)
Six-minute pegboard and ring test
The six minute pegboard and ring test (6-PBRT) will be used to assess upper extremity exercise capacity. The test will be repeated twice on the first and second day evaluations. One week later, the second 6-PBRT test will be performed for reliability analysis.
Time frame: First day and second day
Maximal symptom-limited arm ergometer test
Maximal symptom-limited arm ergometer test will be performed to analyze the validity of the 6-PBRT. The test will be used as the criterion measure for the validity of the six minute peg board and ring test. For the test, the height of the ergometer will be adjusted to be at shoulder level and the test will be performed in a sitting position.
Time frame: First day
Hand-grip strength
For validity the correlation between 6-PBRT and hand grip strength will be examined. Hand grip strength will be assessed using a hand dynamometer. Patients will sit in a 90° upright position with their knees, wrists in neutral, elbows at 90° and the dynamometer attached to the body will be grasped with all their strength. Measurements will be repeated 3 times on the right and left extremities with 10 seconds intervals and the highest value will be recorded. The percentage of expected values determined according to age and gender will be used in the interpretation of the measurements.
Time frame: Second day
Disabilities of the arm, shoulder and hand (DASH) questionnaire
It will be used to evaluate the upper extremity functional status of patients. For validity, the correlation between 6-PBRT and functional status will be examined. Disabilities of the arm, shoulder and hand (DASH) questionnaire evaluates the functional status of the upper extremity subjectively according to the Likert scale. The scale consists of three parts. The questionnaire scores between 0 (no disability) and 100 (severe disability).
Time frame: First day
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Evaluation of pain severity
The severity of the individuals' resting activity and night pain will be questioned with the Visual Analog Scale. The visual analog scale is a scale consisting of a horizontal line of 100 mm length, 0 mm meaning no pain and 100 mm meaning unbearable pain. Individuals will be asked to place a mark on the horizontal line indicating the severity of the pain they feel. The results will be recorded in mm. Individuals will be asked about their resting activity and nighttime localization and will be recorded.
Time frame: First day