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Not yet recruiting NCT07504094

Active Coping: Interdisciplinary Program for Chronic Pain, Physiotherapy Unit (Spain)

No phase Interventional Chronic Back Pain Chronic Pain Back Pain Low Back Pain, Chronic

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Pain Neuroscience Education (PNE), Healthy Habits and Psychological Intervention, Therapeutic Exercise.
Who it may be relevant to
Registry conditions: Chronic Back Pain, Chronic Pain, Back Pain, Low Back Pain, Chronic. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Spain
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Interdisciplinary Active Coping Program for Chronic Pain in the Physiotherapy Unit in Primary Care - Teruel Health Sector (Aragón, Spain)

Overview

The goal of this observational intervention study is to evaluate the impact of a multidisciplinary active coping program for chronic back pain in adults referred from Primary Care to the Physiotherapy Unit of Teruel Ensanche. The main questions it aims to answer are: * Does the program improve physical function, measured through gait speed, balance, and chair stand tests? * Does it reduce pain-related psychological factors such as kinesiophobia, catastrophizing, anxiety, and depression? * Does it improve quality of life and sleep quality, and reduce analgesic medication use? Participants will attend group sessions on pain neuroscience education, followed by sessions on healthy habits, nutrition and sleep hygiene and group psychological intervention focused on emotional wellbeing tools, and will complete therapeutic exercise sessions over the course of the program. They will also complete validated questionnaires and physical assessments at three timepoints: at baseline, at the end of the program, and at a 6-month follow-up.

Interventions

  • Behavioral Pain Neuroscience Education (PNE)
    Group sessions led by primary care physicians aimed at shifting participants' understanding of chronic pain mechanisms, reducing unhelpful beliefs about pain and movement, and promoting active coping strategies. Knowledge is assessed before and after sessions using a validated survey. Timing: March 2026
  • Behavioral Healthy Habits and Psychological Intervention
    Group sessions addressing nutrition and sleep hygiene, combined with group and individual psychological sessions focused on emotional wellbeing and coping tools for chronic pain management. Timing: April 2026
  • Behavioral Therapeutic Exercise
    Timing: May-June 2026 Description: Progressive group therapeutic exercise sessions led by physiotherapists, targeting physical function, balance, gait speed, and strength in participants with chronic back pain.

Primary outcome measures

  • Change from Baseline in Health-Related Quality of Life as Measured by the SF-36 v2 at End of Program and 6-Month Follow-Up [Time frame: Baseline, end of program, 6-month follow-up]
Secondary outcome measures (12)
  • Change from Baseline in Functional Disability as Measured by the Roland-Morris Disability Questionnaire at End of Program and 6-Month Follow-Up [Time frame: Baseline, end of program, 6-month follow-up]
  • Change from Baseline in Physical Performance as Measured by the Short Physical Performance Battery (SPPB) at End of Program and 6-Month Follow-Up [Time frame: Baseline, end of program, 6-month follow-up]
  • Change from Baseline in Dynamic Balance as Measured by the Timed Up and Go Test (TUG) at End of Program and 6-Month Follow-Up [Time frame: Baseline, end of program, 6-month follow-up]
  • Change from Baseline in Lower Limb Strength and Balance as Measured by the 30-Second Sit-to-Stand Test at End of Program and 6-Month Follow-Up [Time frame: Baseline, end of program, 6-month follow-up]
  • Change from Baseline in Gait Speed and Exercise Tolerance as Measured by the 6-Minute Walk Test at End of Program and 6-Month Follow-Up [Time frame: Baseline, end of program, 6-month follow-up]
  • Change from Baseline in Kinesiophobia as Measured by the Tampa Scale for Kinesiophobia (TSK-11SV) at End of Program and 6-Month Follow-Up [Time frame: Baseline, end of program, 6-month follow-up]
  • Change from Baseline in Pain Catastrophizing as Measured by the Pain Catastrophizing Scale (ECD) at End of Program and 6-Month Follow-Up [Time frame: Baseline, end of program, 6-month follow-up]
  • Change from Baseline in Central Sensitization Symptoms as Measured by the Central Sensitization Inventory (CSI) at End of Program and 6-Month Follow-Up [Time frame: Baseline, end of program, 6-month follow-up]
  • Change from Baseline in Analgesic and Co-adjuvant Medication Use as Recorded by Medication Registry at End of Program and 6-Month Follow-Up [Time frame: Baseline, end of program, 6-month follow-up]
  • Change from Baseline in Frequency of Primary Care Consultations (Medical and Physiotherapy) at End of Program and 6-Month Follow-Up [Time frame: Baseline, end of program, 6-month follow-up]
  • Change from Baseline in Anxiety as Measured by the State-Trait Anxiety Inventory (STAI) at End of Program and 6-Month Follow-Up [Time frame: Baseline, end of program, 6-month follow-up]
  • Change from Baseline in Depressive Symptoms as Measured by the Beck Depression Inventory II (BDI-II) at End of Program and 6-Month Follow-Up [Time frame: Baseline, end of program, 6-month follow-up]

Eligibility criteria

Inclusion criteria

  • Adult (18 years or older)
  • Diagnosis of non-oncological chronic back pain
  • Referred from Primary Care to the Physiotherapy Unit of Teruel Ensanche . (UFAP) from one of the following basic health zones: Teruel Centro, Teruel Ensanche, Albarracín, Alfambra, Cella, or Villel
  • Able to provide voluntary written informed consent

Exclusion criteria

  • Oncological pain
  • Cognitive impairment that prevents following the program
  • Spinal surgery in the last year
  • Internal electrostimulator device (e.g. pacemaker, spinal cord stimulator)

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
N/A
Model
Single group
Masking
Open label
Primary purpose
Treatment

Study locations

Spain · 2 centers
  • CS Teruel Centro — Teruel
  • Centro de Salud Teruel Ensanche — Teruel

Publications

  • Louw A, Riera-Gilley V. Pain Neuroscience Education: Teaching People About Pain. J Pain Palliat Care Pharmacother. 2024 Sep;38(3):292-301. doi: 10.1080/15360288.2024.2424853. Epub 2024 Nov 11. PMID 39526886
  • Geneen LJ, Moore RA, Clarke C, Martin D, Colvin LA, Smith BH. Physical activity and exercise for chronic pain in adults: an overview of Cochrane Reviews. Cochrane Database Syst Rev. 2017 Apr 24;4(4):CD011279. doi: 10.1002/14651858.CD011279.pub3. PMID 28436583
  • Galan-Martin MA, Montero-Cuadrado F, Lluch-Girbes E, Coca-Lopez MC, Mayo-Iscar A, Cuesta-Vargas A. Pain Neuroscience Education and Physical Therapeutic Exercise for Patients with Chronic Spinal Pain in Spanish Physiotherapy Primary Care: A Pragmatic Randomized Controlled Trial. J Clin Med. 2020 Apr 22;9(4):1201. doi: 10.3390/jcm9041201. PMID 32331323

Identifiers

NCT: NCT07504094 · C.I.PI26/047

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗