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Neuropathic Pain, Catastrophizing, and Adherence in SAIS

StatusCompleted
PhaseNot specified
Started
View on ClinicalTrials.gov ↗

Record History

  1. Trial completed Final enrollment: 84 participants (planned 75) · Primary completion date changed from estimate of Aug 1, 2026 to Sep 1, 2026 · Eligibility criteria expanded, about 14 words · 3 more Show 6 more changesShow less
    • Final enrollment: 84 participants (planned 75)
    • Primary completion date changed from estimate of Aug 1, 2026 to Sep 1, 2026
    • Eligibility criteria expanded, about 14 words
    • Secondary endpoints: details revised at 6 of 6 entries
    • Site details revised
    • Publications: details revised at 2 of 3 entries
  2. Recruitment opened Start date changed from estimate of Apr 1, 2026 to Apr 2, 2026 · Site details revisedv2 Show 2 more changesShow less
    • Start date changed from estimate of Apr 1, 2026 to Apr 2, 2026
    • Site details revised
  3. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
Subacromial impingement syndrome is one of the most common causes of shoulder pain and may negatively affect daily activities and quality of life. While shoulder pain is usually considered nociceptive, some patients may also have a neuropathic pain component, which can influence symptom severity and treatment outcomes. In addition, psychological factors such as pain catastrophizing and adherence-related behavior may play an important role in recovery. This prospective observational study aims to evaluate the presence of neuropathic pain in patients with subacromial impingement syndrome and to investigate its relationship with pain catastrophizing and adherence-related behavior. Patients undergoing a standard physical therapy program will be assessed at the beginning and after completion of treatment using validated clinical scales. The findings of this study may help to better understand the interaction between pain characteristics, psychological factors, and adherence-related behavior, and contribute to the development of more individualized rehabilitation strategies
Trial Details
NCT Number NCT07509021
Lead Sponsor Abant Izzet Baysal University
Conditions Subacromial Impingement Syndrome
Enrollment 84 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov