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Biopsychosocial vs Multimodal Chronic Pain Management

CompletedNot applicableNCT07406711
View the official record on ClinicalTrials.gov

Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.

This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.

Brief summary (from the registry)

This study evaluated the effects of a multidisciplinary biopsychosocial program compared with standard multimodal care in patients with chronic low back pain treated at the University Hospital Osijek. Outcomes included pain intensity, disability, health-related quality of life, anxiety, depression, stress, and sleep quality. Data were collected using standardized self-assessment questionnaires and objective monitoring of sleep and physical activity during a four-week intervention period. The study was conducted as part of a doctoral dissertation.

Study details

Official title
Randomized Controlled Trial on the Effectiveness of a Multidisciplinary Biopsychosocial Program vs Multimodal Treatment in Patients With Chronic Low Back Pain
Conditions
Interventions
  • Behavioral: Four-week program including group and individual therapy with a multidisciplinary team.Sessions included educational lectures, physical therapy, and multimodal interventions.
  • Other: Multimodal treatment. Four-week program including: TENS
  • Therapeutic ultrasound
  • Magnetotherapy
  • Acupuncture. Participants continued their usual prescribed medications.
Sponsor
Osijek University Hospital
Collaborators
Josip Juraj Strossmayer University of Osijek
Start date
2021-11-15
Primary completion
2023-05-29
Sex
All
Age range
from 18 Years to 65 Years
Results posted
No results posted in this snapshot
Countries
Croatia
Total sites listed
1

Eligibility criteria

Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * Age 18-65 years * Chronic low back pain significantly affecting disability and/or emotional distress * Active use of Croatian language * Signed informed consent Exclusion Criteria: * Age \<18 or \>65 * Acute pain * Previous participation in multidisciplinary program * Pregnancy or cancer-related pain * Psychotic disorders, moderate-severe cognitive impairment, urgent psychiatric conditions * PTSD symptoms, extreme fatigue, low motivation, low literacy * Allergic reactions to metal or silicone

Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT07406711