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Effectiveness of an Interdisciplinary Pain Education Program in Public Health: a Pragmatic Clinical Trial

Not Applicable
Not yet recruiting
Conditions
Musculoskeletal Pain
Interventions
Behavioral: Interdisciplinary Pain Education Program
Other: Conventional Physiotherapy treatment
Registration Number
NCT05544383
Lead Sponsor
Federal University of Espirito Santo
Brief Summary

The objective of this study is to evaluate the effectiveness of an interdisciplinary pain education program in improving self-efficacy and promoting quality of life in patients with chronic musculoskeletal pain in public health. This is a pragmatic clinical trial carried out with patients referred to the Physical Therapy sector of a municipality who will be allocated in an interdisciplinary pain education intervention group or a comparison group of conventional physical therapy treatment.

Detailed Description

his is a pragmatic clinical trial carried out with patients referred to the Physical Therapy sector of a municipality who will be allocated in an interdisciplinary pain education intervention group or a comparison group of conventional physical therapy treatment. Clinical characteristics of pain will be evaluated by multidimensional questionnaires, in addition to self-efficacy, quality of life, functional literacy and sociodemographic profile. Health professionals will be evaluated by an attitude towards pain inventory. It is expected to demonstrate the effectiveness of interdisciplinary pain education work in managing the biopsychosocial impacts of pain by promoting knowledge and self-management strategies in the care of this chronic condition. As it is a light and collective technology, it can reduce the burden of the disease and support public policy decision-making in the management of chronic pain in public health.

Recruitment & Eligibility

Status
NOT_YET_RECRUITING
Sex
All
Target Recruitment
108
Inclusion Criteria
  • Patients with a clinical picture of chronic musculoskeletal pain, aged over 18 years, being SUS users referred for Physiotherapy treatment.
Exclusion Criteria
  • Patients with a clinical picture of acute pain, post-traumatic or post-surgical pain, cancer pain and neuropathic pain, as well as those with autoimmune diseases. Patients with cognitive problems who cannot understand and respond to the questionnaires and who also have other physical disabilities unrelated to the chronic pain condition.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Intervention groupInterdisciplinary Pain Education ProgramInterdisciplinary Pain Education Program and conventional physical therapy treatment
Comparison groupConventional Physiotherapy treatmentConventional physical therapy treatment
Intervention groupConventional Physiotherapy treatmentInterdisciplinary Pain Education Program and conventional physical therapy treatment
Primary Outcome Measures
NameTimeMethod
Pain Self-Efficacy Questionnaire3 months

The total score is calculated by adding the scores for each of the 10 items, resulting in a value ranging from 0 to 60, with higher scores reflecting stronger self-efficacy beliefs.

Secondary Outcome Measures
NameTimeMethod
Brief Pain Inventory3 months

pain-related scores ranging from zero (did not interfere) to ten (completely interfered)

Health Literacy Scale (HLS-14)3 months

assesses the level of health literacy through fourteen questions on a five-point Likert scale, in three dimensions of literacy: functional and communicative with 5 items each, and critical with 4 items.

Survey of Pain Attitudes-Professionals (IAD-Profissionais)1 day

20 items, covering 6 domains: emotion, control, disability, solicitude, medical cure and physical harm

EuroQol (EQ-5D-3L)3 months

patient's quality of life through self-assessment in five dimensions: mobility; self-care; usual activities; pain/discomfort; anxiety / depression. Each dimension has 3 levels: no problems, some problems, extreme problems/disability

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