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Clinical Trials/NCT06248372
NCT06248372
Not yet recruiting
Not Applicable

The Investigation of the Effects of Attentional Focus Strategies on Pain, Disability, Posture, Quality of Life, and Depression in Patients With Myofascial Pain Syndrome

Yeditepe University0 sites34 target enrollmentJanuary 30, 2024

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Myofascial Pain Syndrome
Sponsor
Yeditepe University
Enrollment
34
Primary Endpoint
Numeric Pain Rating Scale (NPRS)
Status
Not yet recruiting
Last Updated
2 years ago

Overview

Brief Summary

Attentional focus is a concept of motor learning and the usage of this concept promotes exercise-induced muscular adaptations and affects motor performances. In practice,two main verbal instructions are directing the focus of attention; external focus (EFA) and internal focus of attention (IFA). Several studies show the results related with different health conditions. However, there is not enough studies to investigate the effectiveness of these attentional focus strategies in exercise regimes in patients with musculoskeletal problem. Thus, the study will be the first to investigate the effectiveness of attentional focus strategies in patients with neck and upper back myofascial pain syndrome (MPS) which is the most common syndrome of musculoskeletal problems.

Detailed Description

When investigating the literature studies, there is insufficient evidence to determine which attentional focus strategies are more effective for improving function and decreasing pain in different health conditions. In most of the studies duration of symptoms of patients was not mentioned and there are no studies that directly compare EFA and IFA and report the effects on pain or functional outcomes in musculoskeletal conditions.Additionally, one study investigated the effectiveness of attentional focus strategies used in a training program but not in a musculoskeletal problem. Thus, the study aims to investigate the effectiveness of attentional focus strategies in patients with neck and upper back MPS in terms of pain, pressure pain threshold, quality of life, depression, disability, and posture parameters.

Registry
clinicaltrials.gov
Start Date
January 30, 2024
End Date
September 1, 2024
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Yagmur Barlas

Master Degree Student

Yeditepe University

Eligibility Criteria

Inclusion Criteria

  • Symptomatic MPS in the neck and upper back region (upper and middle trapezius, levator scapulae, rhomboids, infraspinatus, and supraspinatus muscles) confirmed by a physician,
  • Pain lasting more than 3 months with a pain intensity is 3 or higher according to numeric pain rating scale (NPRS⩾3).

Exclusion Criteria

  • Fibromyalgia syndrome, cervical disc pathologies, malignancy, neurologic and/or inflammatory diseases, history of neck, shoulder, upper back surgery and trauma, other medical conditions that limit participation in exercise.
  • Pregnancy
  • Individuals being involved in physiotherapy or exercise sessions for at least 4 weeks

Outcomes

Primary Outcomes

Numeric Pain Rating Scale (NPRS)

Time Frame: through study completion;an average 8 months

It is a common scale to measure the perceived level of pain intensity on a numeric scale that usually includes 11 numbers. The participant is instructed to select the number that best reflects the intensity of pain experienced, with 0 representing one extreme of pain (e.g., no pain) and 10 representing the other extreme (e.g., pain as bad as it could be).

Pressure Pain Threshold (PPT)

Time Frame: through study completion;an average 8 months

A digital algometer (Jtech Medical Commander Echo) will be applied to measure the pressure pain threshold of the four most painful myofascial trigger points on both sides of the upper and middle trapezius, levator scapulae, rhomboids, infraspinatus, and supraspinatus. It has a circular flat tip of 1 cm2 which will be pushed slowly to the skin over the trigger points after exploration of a taut band with a normalized speed until the subject presses a switch when the compression sensation alters to pain. This process will repeat three times with a 30-second rest in between and their average will be considered as pressure pain threshold.

Secondary Outcomes

  • New York Posture Rating Chart (NPRC)(through study completion;an average 8 months)
  • Neck Disability Index (NDI)(through study completion;an average 8 months)
  • Beck Depression Inventory (BDI)(through study completion;an average 8 months)
  • SF-12 Questionnaire (SF-12)(through study completion;an average 8 months)

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