Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06052384

Optimization of the Care Pathway for Patients With Chronic Pain: Assessing the Value of Integrating Sleep Specialists

Led by Centre Hospitalier Emile Roux · Updated on 2025-07-30

664

Participants Needed

1

Research Sites

181 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

DOLOREPIT is an interventional, RIPH 2, multicenter, randomized, controlled, open-label study comparing two care pathways for the management of patients with chronic pain.

CONDITIONS

Official Title

Optimization of the Care Pathway for Patients With Chronic Pain: Assessing the Value of Integrating Sleep Specialists

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • First consultation at the pain management center
  • Chronic pain as defined by the Haute Autorité de Santé, with characteristics including persistence or recurrence, duration over 3 months, inadequate treatment response, and significant daily functional deterioration
  • Diagnosis of chronic primary pain classified as chronic generalized pain, complex regional pain syndrome, chronic primary headache or orofacial pain, or chronic primary musculoskeletal pain
  • Completion of the Pittsburgh Sleep Quality Index with score available for randomization
  • Access to an internet connection for completing online questionnaires and online cognitive behavioral therapy if insomnia is detected
  • Affiliation to a French social security system
  • Provided free informed consent
Not Eligible

You will not qualify if you...

  • Receiving cancer treatment or completed cancer treatment within the last 2 years
  • Having a chronic inflammatory disease such as rheumatoid arthritis, ankylosing spondylitis, chronic inflammatory bowel disease, Horton's disease, Wegener's disease, myositis, Still's disease, or lupus erythematosus
  • Being immunocompromised
  • Having severe psychiatric illness preventing study follow-up
  • Already treated by a sleep specialist for a sleep disorder (hypnotic use alone does not exclude)
  • Difficult follow-up due to geographic or other reasons
  • Under judicial protection or guardianship
  • Refusal to participate in the research

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Centre Hospitalier Emile Roux

Le Puy-en-Velay, France

Actively Recruiting

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How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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