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

Active, not recruitingNCT05925192
View the official record on ClinicalTrials.gov

Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.

This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.

Brief summary (from the registry)

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.

Study details

Official title
Profile of Chronic Musculoskeletal Pain Patients Related to Treatment Adherence and Virtual Reality
Interventions
  • Other: Observational study
Sponsor
Universidad de Granada
Start date
2023-06-30
Primary completion
2024-09-30
Sex
All
Age range
from 18 Years to 100 Years
Results posted
No results posted in this snapshot
Countries
Spain
Total sites listed
1

Eligibility criteria

Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * 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 Exclusion Criteria: 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.

Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT05925192