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临床试验/NCT07838233
NCT07838233尚未招募不适用

Development and Psychometric Evaluation of a Night Pain Module in Rotator Cuff-Related Shoulder Pain

Istanbul Physical Medicine Rehabilitation Training and Research Hospital3 个研究点 分布在 1 个国家目标入组 275 人开始时间: 2026年10月1日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
275
试验地点
3
主要终点
Psychometric Properties of the Night Pain Module

研究概览

简要总结

Night pain is common in people with rotator cuff-related shoulder pain and may disturb sleep and daily life. It may include difficulty falling asleep, waking because of pain, increased pain during the night, difficulty returning to sleep, and pain when lying on the affected shoulder. However, night pain is often assessed with only one pain score or a yes/no question.

This study aims to develop and evaluate a short Night Pain Module for people with rotator cuff-related shoulder pain. The current draft contains eight items assessing different features of night pain during the previous seven days. The items may be revised after expert review and pilot testing. The validity and reliability of the final version will be examined in the main study. A subgroup of participants will complete the module again after 7-10 days. No treatment or experimental procedure will be given as part of the study.

详细描述

Night pain is an important symptom in rotator cuff-related shoulder pain. It may affect falling asleep, cause waking during the night, increase the need to change position, and make it difficult to return to sleep. Pain may also increase when the person lies on the affected shoulder. These features may not be fully described by a single pain score. This study aims to develop a short and practical Night Pain Module that can assess the different features of night pain in clinical practice and research.

The current draft of the Night Pain Module contains eight items. These items assess difficulty falling asleep because of shoulder pain, the number of nights with pain-related waking, pain intensity at the time of waking, average shoulder pain during the night, increased pain when lying on the affected shoulder, pain relief after changing position, the need to change position because of pain, and difficulty returning to sleep after waking because of shoulder pain. Participants will answer the items based on their experience during the previous seven days. The number and wording of the items may be revised after expert panel review and pilot testing.

The development process will have three stages. First, the draft items will be reviewed by a multidisciplinary panel of 20 experts, including specialists in physical medicine and rehabilitation, orthopedics and traumatology, algology, and psychiatry. The experts will rate each item for clinical relevance, clarity, and ability to represent night pain. Their ratings will be used to assess content validity and to revise or remove items when necessary.

Second, the revised module will be tested in a pilot group of approximately 20-30 participants. The pilot assessment will examine whether the items are easy to understand, how long the module takes to complete, whether any items are frequently left unanswered, and whether responses are concentrated at the lowest or highest possible scores. The pilot data will not be included in the main psychometric analyses. Necessary changes will be made before the final version is used in the main study.

Third, the final version of the Night Pain Module will be evaluated in the main study sample. Its structure will be examined using exploratory and confirmatory factor analyses. These analyses will assess whether the items measure one general night pain concept or separate features, such as sleep-disturbing pain and position-related pain. Internal consistency and item-total relationships will also be evaluated.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 60 Years(Adult)
性别
All
接受健康志愿者
否

入选标准

  • •nclusion Criteria:
  • •Age between 18 and 60 years
  • •Shoulder pain lasting for at least six weeks
  • •Anterolateral shoulder pain
  • •Clinical diagnosis of rotator cuff-related shoulder pain based on at least two positive results among the following tests:
  • •Neer test Hawkins-Kennedy test Jobe (Empty Can) test Painful Arc test Resisted External Rotation test
  • •Willingness to participate and ability to provide written informed consent

排除标准

  • •Clinically evident frozen shoulder with restricted passive external rotation
  • •Shoulder injection within the previous four weeks
  • •Cervical radiculopathy
  • •Acute shoulder trauma
  • •Marked muscle weakness suggesting a full-thickness rotator cuff tear
  • •Calcific tendinitis
  • •Neurological or systemic disease that prevents participation
  • •Pregnancy, postpartum period, or breastfeeding
  • •Inability to provide informed consent

研究组 & 干预措施

Adults With Rotator Cuff-Related Shoulder Pain

Adults aged 18-60 years with shoulder pain lasting at least six weeks and a clinical diagnosis of rotator cuff-related shoulder pain. The diagnosis will be based on anterolateral shoulder pain and at least two positive clinical provocation tests. The study includes a single patient cohort without a healthy control group or an assigned intervention.

结局指标

主要结局

Psychometric Properties of the Night Pain Module

时间窗: Baseline and 7-10 days after baseline for the retest subgroup

The validity and reliability of the final Night Pain Module will be evaluated. Content validity will be examined using item-level and scale-level content validity indices. Structural validity will be assessed using exploratory and confirmatory factor analyses. Internal consistency will be evaluated using Cronbach's alpha and item-total correlations. Test-retest reliability will be assessed using the intraclass correlation coefficient in clinically stable participants who complete the module again after 7-10 days.

次要结局

  • Relationship Between Night Pain Module Scores and Sleep Quality(Baseline)
  • Relationship Between Night Pain Module Scores and Shoulder Pain and Disability(Baseline)
  • Relationship Between Night Pain Module Scores and Pain Catastrophizing(Baseline)

研究者

发起方
Istanbul Physical Medicine Rehabilitation Training and Research Hospital
申办方类型
Other Gov
责任方
Principal Investigator
主要研究者

Eser Kalaoglu

Associate Professor of Physical Medicine and Rehabilitation

Istanbul Physical Medicine Rehabilitation Training and Research Hospital

研究点 (3)

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