Actively Recruiting

Age: 18Years - 65Years
All Genders
ID07509021

Relationship Between Neuropathic Pain, Pain Catastrophizing, and Adherence-Related Behavior in Subacromial Impingement Syndrome Observational Study

Led by Abant Izzet Baysal University · Updated on 2026-04-08

75

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Subacromial impingement syndrome is a common cause of shoulder pain that can affect daily life and quality of life. This research aims to evaluate the presence of neuropathic pain in patients with this condition and to explore how it relates to pain catastrophizing and behaviors related to treatment adherence. The study is a prospective observational cohort conducted by Abant Izzet Baysal University to better understand these interactions and support personalized rehabilitation strategies. Participants diagnosed with subacromial impingement syndrome will undergo a standard conservative physical therapy program as part of routine care. No experimental treatments will be given. The study will assess neuropathic pain and pain catastrophizing at the start and after two weeks of therapy. Secondary measures include pain intensity at rest, during activity, and at night, functional status, anxiety and depression levels, and adherence-related behavior. During the study, patients will be evaluated at baseline and after completing the physical therapy program using clinical and patient-reported outcome measures. Assessments include validated scales for neuropathic pain, pain catastrophizing, pain intensity, functional ability, psychological status, and adherence behaviors. The study will help clarify how these factors relate and may guide more individualized treatment approaches. Participants will be involved for approximately two weeks during their therapy course.

CONDITIONS

Brief Title

Neuropathic Pain, Catastrophizing, and Adherence in SAIS

Who Can Participate

Age: 18Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 18 to 65 years
  • Diagnosed with unilateral subacromial impingement syndrome lasting at least 3 months
  • Planned to start a 10-session physical therapy program
  • Willing and able to provide informed consent
Not Eligible

You will not qualify if you...

  • Upper extremity entrapment neuropathy or polyneuropathy
  • History of diabetes mellitus
  • Inflammatory rheumatic disease, infection, or malignancy
  • Frozen shoulder
  • History of shoulder fracture, dislocation, or surgery
  • Complete rotator cuff tear on magnetic resonance imaging
  • Calcific tendinitis
  • Shoulder steroid injection or physical therapy within the previous 3 months
  • Use of medication for neuropathic pain
  • Pregnancy
  • Cognitive impairment preventing completion of questionnaires

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Monitoring

Duration - Approximately 2 weeks

Participants who undergo routine care are observed to assess neuropathic pain, pain catastrophizing, adherence-related behavior, and clinical outcomes during a standard conservative physical therapy program.

2 visits (baseline and 2-week follow-up)

Trial Site Locations

Total: 1 location

1

AIBU Izzet Baysak Physical Treatment and Rehabilitation Hospital

Bolu, Turkey (Türkiye), 14020

Actively Recruiting

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Research Team

Y

Yakup ERDEN, MD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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