ClinicalTrials.Veeva

Menu

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

C

Centre Hospitalier Emile Roux

Status

Enrolling

Conditions

Chronic Pain

Treatments

Other: Standard pain management combined with sleep disorder management

Study type

Interventional

Funder types

Other

Identifiers

NCT06052384
RIPH2_PEREZ_DOLOREPIT
2022-A00919-34 (Other Identifier)

Details and patient eligibility

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.

Enrollment

664 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • First consultation at the pain management center

  • Patient with chronic pain as defined by the "Haute Autorité de Santé". The pain must have several of the following characteristics:

    • Persistence or recurrence
    • Duration beyond what is usual for the presumed initial cause, especially if the pain has been evolving for more than 3 months;
    • Inadequate response to treatment;
    • Important and progressive deterioration of the patient's functional and interpersonal abilities in activities of daily living at home, school, or work due to the pain.
  • Patients with chronic primary pain (according to the typology defined by the International Classification of Diseases-11) and classified into one of the 4 following categories:

    • Chronic generalized pain
    • Complex regional pain syndrome
    • Chronic primary headache or orofacial pain
    • Chronic primary musculoskeletal pain
  • Pittsburgh Sleep Quality Index (PSQI) must be completed by the patient and the score must be available (for randomization purposes)

  • Have access to an internet connection as a self-administered questionnaire is to complete online, and at least have access to the online platform for CBT treatment if insomnia is detected

  • Affiliation to a French social security system

  • Free informed consent

Exclusion criteria

  • Patients undergoing cancer treatment or who have completed treatment within the last 2 years
  • Patient with a chronic inflammatory disease (e.g. rheumatoid arthritis, ankylosing spondylitis, chronic inflammatory bowel disease, Horton's disease, Wegener's disease, myositis, Still's disease, lupus erythematosus, etc.)
  • Immunocompromised patient
  • Patient with severe psychiatric pathology that does not allow study follow-up (at the discretion of the investigator)
  • Patient already treated for a sleep disorder by a sleep specialist (the only prescription of hypnotics is not considered as a criterion of non-inclusion)
  • Patient follow-up difficult (for geographic motives or other reasons)
  • Patient under judicial protection of incapable adults or guardianship
  • Refusal to participate in the research

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

664 participants in 2 patient groups

Reinforced sleep program
Experimental group
Description:
standard pain management + sleep disorders management
Treatment:
Other: Standard pain management combined with sleep disorder management
Standard care
No Intervention group
Description:
Control group: standard pain management

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems