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临床试验/NCT06506604
NCT06506604已完成不适用

"Psychological Intervention Enhanced by Virtual Reality for the Improvement of Appreciation of Body Functionality in Patients With Chronic Low-back-pain".

University of Valencia2 个研究点 分布在 1 个国家目标入组 13 人开始时间: 2024年6月3日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
13
试验地点
2
主要终点
Body Disability

研究概览

简要总结

The purpose of this study is to test whether a positive body image-based intervention is able to improve pain, disability, interference and emotional distress in people with chronic low back pain.

Patients will receive 4 sessions approaching 5 different clinical modules: Pain Psychoeducation, Body Awareness, Pain Acceptance, Body Appreciation and Functionality and Gratitude. 2 sessions will include virtual reality (VR) environments to enhance the clinical outcomes.

Researchers will analyse changes in the variables of interest after intervention compared to baseline.

详细描述

The purpose of this intervention is to examine the effects of a positive body image-based intervention using virtual reality to improve pain, interference and emotional distress.

The first session will be dedicated to psychoeducation about pain. Investigators will discuss what chronic pain is, what factors influence pain, chronification, body image and a brief presentation of the modules.

In the second session, a brief introduction to body awareness will be given and a VR environment will be used to carry out a body scan.

In the third session, Acceptance of pain will be worked on and a VR environment will be used to work on some variables related to the chronification of pain, such as paradoxical control or avoidance.

In the fourth session, the modules of Appreciation and Gratitude will be addressed.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Participant)

盲法说明

Participants are blind to the variables of change.

入排标准

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

入选标准

  • Individuals with low back pain.

排除标准

  • Meeting any of the following medical conditions:
  • Spinal tumor, infection or fracture
  • Systemic disease (autoimmune, infectious, vascular, endocrine, metabolic...)
  • Fibromyalgia
  • Cauda equina syndrome
  • History of spinal surgery
  • Musculoskeletal injury of lower extremities

结局指标

主要结局

Body Disability

时间窗: The whole scale will be administered at the beginning (day 1 of 43) and the end of the intervention (day 43 of 43).

Roland-Morris Questionnaire (RMQ) is a 24-item patient-reported outcome measure those inquiries about pain-related disability. Items are scored 0 if left blank or 1 if endorsed, for a total RMQ score ranging from 0 to 24.

Pain Interference and Pain Intensity

时间窗: The whole scale will be administered at the beginning (day 1 of 43) and the end of the intervention (day 43 of 43).

The Brief Pain Inventory (BPI) scale was developed to assess the severity of pain and its impact on functioning. The scale consists of 9 items with qualitative and quantitative data on the following dimensions: "Worst pain in last 24 hours", "Least pain in last 24 hours", "Pain on average" and "Pain right now".

Emotional Distress

时间窗: The whole scale will be administered at the beginning (day 1 of 43) and the end of the intervention (day 43 of 43).

The 4-item Brief Assessment of Distress about Pain (BADP) scale was developed to assess anxiety, fear, and depression related to pain, as well as an overall evaluation of distress about pain. Items are scored from 0 ("Not at all") to 4 ("Extreme"), for a total BADP score ranging from 0 to 16.

Level of Quality of Life

时间窗: The whole scale will be administered at the beginning (day 1 of 43) and the end of the intervention (day 43 of 43).

The EuroQol-5D (EQ-5D) scale is a 5-item scale to assess the quality of life of patients with several pathologies, chronic pain included. The individual assesses his or her own state of health, first in levels of severity by dimensions (descriptive system) and then on a more general visual analogue scale (VAS).

次要结局

  • Chronic Pain Acceptance(The whole scale will be administered at the beginning (day 1 of 43) and the end of the intervention (day 43 of 43).)
  • Fear of movement(The whole scale will be administered at the beginning (day 1 of 43) and the end of the intervention (day 43 of 43).)
  • Body Awareness(The whole scale will be administered at the beginning (day 1 of 43) and the end of the intervention (day 43 of 43).)
  • Body Appreciation(The whole scale will be administered at the beginning (day 1 of 43) and the end of the intervention (day 43 of 43) and one of the items of the scale -'I FEEL LOVE AND RESPECT FOR MY BODY'- will be administered daily for 43 days via MPATH.)
  • Appreciation of Body Functionality(The whole scale will be administered at the beginning (day 1 of 43) and the end of the intervention (day 43 of 43).)
  • Pain Catastrophizing(The whole scale will be administered at the beginning (day 1 of 43) and the end of the intervention (day 43 of 43).)
  • Depression(The whole scale will be administered at the beginning (day 1 of 43) and the end of the intervention (day 43 of 43).)
  • Anxiety(The whole scale will be administered at the beginning (day 1 of 43) and the end of the intervention (day 43 of 43).)

研究者

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

Rosa M. Baños Rivera

Full Professor

University of Valencia

研究点 (2)

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