Multidisciplinary Intervention for Non-Cancer Chronic Pain: Pilot Study

NCT ID: NCT07273084

Last Updated: 2025-12-17

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

ACTIVE_NOT_RECRUITING

Clinical Phase

NA

Total Enrollment

12 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-07-01

Study Completion Date

2026-03-01

Brief Summary

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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.

Detailed Description

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Conditions

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Non-cancer Pain Chronic Non-cancer Pain

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Experimental: Multidisciplinary Intervention

All participants will receive a multidisciplinary intervention program lasting 6 weeks, consisting of 17 sessions that combine pain neuroscience education, individualized therapeutic exercises, and promotion of healthy lifestyle habits. The program aims to improve pain management skills and health-related quality of life in patients with non-cancer chronic pain.

Group Type EXPERIMENTAL

Multidisciplinary Intervention Program for Chronic Non-Cancer Pain

Intervention Type BEHAVIORAL

A 6-week multidisciplinary group program composed of 17 sessions combining pain neuroscience education, individualized therapeutic exercises, and promotion of healthy lifestyle habits. The intervention aims to improve pain management skills, physical function, and health-related quality of life in adults with non-cancer chronic pain.

Interventions

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Multidisciplinary Intervention Program for Chronic Non-Cancer Pain

A 6-week multidisciplinary group program composed of 17 sessions combining pain neuroscience education, individualized therapeutic exercises, and promotion of healthy lifestyle habits. The intervention aims to improve pain management skills, physical function, and health-related quality of life in adults with non-cancer chronic pain.

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* Individuals aged between 18 and 79 years.
* Individuals diagnosed with non-cancer chronic pain lasting more than 3 months.

Exclusion Criteria

* Individuals with pain of oncologic origin.
* Individuals who have experienced a fracture or undergone surgery within the past year.
* Pregnant women.
* Individuals without adequate understanding of the Spanish language.
* Individuals with cognitive impairment that prevents them from performing the program's interventions.
* Individuals with physical performance deficits that prevent them from carrying out the program's activities.
* Individuals with urinary and/or fecal incontinence.
Minimum Eligible Age

18 Years

Maximum Eligible Age

79 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Victor Ortiz Mallasen

OTHER

Sponsor Role lead

Responsible Party

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Victor Ortiz Mallasen

Assistant Professor of Nursing

Responsibility Role SPONSOR_INVESTIGATOR

Locations

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Benicassim Health Center

Benicassim, Castellón, Spain

Site Status

Countries

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Spain

Other Identifiers

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PILOT-12PAT-2025

Identifier Type: -

Identifier Source: org_study_id