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NCT07273084: MICNP

Multidisciplinary Intervention for Non-Cancer Chronic Pain: Pilot Study

Active, enrolled NA Last updated 17 December 2025
What this trial tests

NA trial testing Multidisciplinary Intervention Program for Chronic Non-Cancer Pain in Non-cancer Pain in 12 participants. Participants enrolled and being followed up; not accepting new ones.

Timeline
1 July 2025
Primary endpoint
1 September 2025
1 March 2026

Quick facts

Lead sponsorVictor Ortiz Mallasen
PhaseNA
StatusActive, enrolled
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment12
Start date1 July 2025
Primary completion1 September 2025
Estimated completion1 March 2026
Sites1 location across Spain

Drugs / interventions tested

Conditions studied

Sponsor

Victor Ortiz Mallasen

Who can join

Adults 18 to 79, any sex, with Non-cancer Pain or Chronic Non-cancer Pain. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Introduction: Non-cancer chronic pain (NCCP) persists beyond the injury that caused it, affecting approximately 20% of the global population (around 1.6 billion people) and 17-18% in Spain (about 8 million people). Its treatment is complex and often insufficient, highlighting the need for an integrated, multimodal, multidisciplinary approach coordinated between primary and hospital care. Objective: To evaluate the effectiveness of a multidisciplinary intervention program combining pain neuroscience education, therapeutic physical exercise, and promotion of healthy habits, aiming to improve health-related quality of life in individuals with NCCP at the Benicàssim Health Center. Methodology: This is a quasi-experimental, before-and-after pilot study, non-randomized, without a control group, using a convenience sample of 12 participants. Sociodemographic, health-related, and clinical variables will be measured, including health-related quality of life, central sensitization, kinesiophobia, catastrophizing, pain level, body mass index, sleep quality, perceived social support, anxiety, and depression. Measurements will be taken before the program, at completion, and at 3 months. The intervention is a 6-week group program with 17 sessions, combining pain neuroscience education, individualized therapeutic exercises, and promotion of healthy habits. Data will be analyzed using SPSS v.29 with a significance level of p\<0.05.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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