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临床试验/NCT05925192
NCT05925192招募中不适用

Profile of Chronic Musculoskeletal Pain Patients Related to Treatment Adherence and Virtual Reality

Universidad de Granada1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2023年6月30日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
100
试验地点
1
主要终点
Neurophysiology of Pain

研究概览

简要总结

Lack of adherence is one of the main problems of chronic musculoskeletal pain treatment. To improve adherence it is essential to take into account the characteristics of the patients and their thoughts and beliefs about pain. Virtual reality can present some advantages in the face of these problems too.

The objective of this study is to evaluate the profile of chronic musculoskeletal pain patients, the barriers associated with lack of adherence to treatment, and the interest of virtual reality in rehabilitation.

详细描述

  • Background: Lack of adherence is one of the main problems of chronic musculoskeletal pain treatment. To improve adherence it is essential to take into account the characteristics of the patients and their thoughts and beliefs about pain. Virtual reality can present some advantages in the face of these problems too.
  • Objectives: Evaluate the profile of chronic musculoskeletal pain patients, the barriers associated with lack of adherence to treatment, and the interest of virtual reality in rehabilitation.
  • Methodology: Observational study. The profile of chronic musculoskeletal pain patients will be described. Patients will be recruited using the snowball method. The evaluation will be carried out via telematics through the use of videoconference and surveys. We will evaluate chronic pain and characteristics, kinesiophobia, functionality, quality of life, psychosocial aspects and other related outcomes. We will identify barriers associated to treatment adherence and we will evaluate patients' perception of rehabilitation with virtual reality.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Cross Sectional

入排标准

年龄范围
18 Years 至 100 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Chronic musculoskeletal pain (≥ 3 months)
  • Adults (≥ 18 years)
  • Have a computer or mobile device/Basic knowledge and access to the internet
  • Wish to participate in the study and sign the informed consent

排除标准

  • All those participants who present any physical pathology or of any kind that imply an inability to understand the necessary instructions to carry out the study will be excluded.

结局指标

主要结局

Neurophysiology of Pain

时间窗: Baseline

To assess neurophysiology of pain using the neurophysiology of pain questionnaire. Scores range from 0 to 13 (sum of all correct items).

Pain Intensity

时间窗: Baseline

To assess pain intensity using the verbal numeric pain scale. Scores range from 0 (no pain) to 10 (worst pain imaginable). Higher scores indicate greater intensity.

Pain Severity

时间窗: Baseline

To assess pain severity using the brief pain inventory. Scores range from 0 (no pain/does not interfere) to 10 (worst pain imaginable/completely interferes). Higher scores indicate greater severity.

Pain Intensity and chronic pain interference

时间窗: Baseline

To assess pain intensity and chronic pain interference using the graded chronic pain scale. Scores range from 0 (no pain/no interference) to 10 (worst pain imaginable/unable to carry on any activities). Higher scores indicate greater intensity or interference.

Chronic Pain Acceptance

时间窗: Baseline

To assess chronic pain acceptance using the chronic pain acceptance questionnaire. Scores range from 0 (never true) to 6 (it is always true). Higher scores indicate greater acceptance.

Awareness, Consciousness, Vigilance and Observation of pain

时间窗: Baseline

To assess awareness, consciousness, vigilance and observation of pain using the pain vigilance and awareness questionnaire. Scores range from 0 (never) to 5 (always). The total questionnaire scores range between 0 and 80. Higher scores indicate greater awareness, consciousness, vigilance and observation of pain.

次要结局

  • Kinesiophobia(Baseline)
  • Catastrophizing of pain(Baseline)
  • Functionality(Baseline)
  • Health-related Quality of Life(Baseline)
  • Work performance(Baseline)
  • Disability(Baseline)
  • Level of movement related to space(Baseline)
  • Physical activity(Baseline)
  • Patients' perception to virtual reality rehabilitation(Baseline)
  • Sleep Quality(Baseline)
  • Depression and anxiety(Baseline)
  • Social support(Baseline)
  • Treatment information and barriers associated to treatment adherence(Baseline)
  • Barriers associated to doing exercise therapy(Baseline)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Irene Torres Sánchez

PT, PhD, Principal investigator

Universidad de Granada

研究点 (1)

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