Effect of BETY on Biopsychosocial States Associated With Chronic Pain in Rheumatic Individuals.

NCT06702839 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 300

Last updated 2025-12-02

No results posted yet for this study

Summary

No study has been found in the literature investigating the effectiveness of an innovative exercise approach defined on a biopsychosocial basis and having its own original scale on individuals with rheumatism over the years. The aim of this retrospective study was to determine the effects of the Cognitive Exercise Therapy Approach on the biopsychosocial conditions related to chronic pain; functionality, mood and quality of life of individuals with rheumatism diagnosis and to examine the effectiveness of BETY as a routine exercise approach by presenting the results compared with the control group.

Conditions

  • Rheumatic Diseases

Interventions

OTHER

BETY (Cognitive Exercise Therapy Approach )

Individuals with rheumatism were included in BETY sessions after the first session, which included functional gain with function-focused trunk stabilization exercises for their complaints and chronic pain management training based on neuroscience. BETY sessions included function-focused trunk stabilization exercises, chronic pain management, mood information management (dance therapy - authentic movement) as innovative. Individuals were included in a separate session of sexual information management and sleep education. 3 days a week for 3 months

OTHER

Home exercise program

Exercises have been shown and a brochure has been given The individuals in this group were mostly individuals from out of town who were given home exercise recommendations directed by a rheumatologist.

Sponsors & Collaborators

  • Hacettepe University

    collaborator OTHER
  • Eastern Mediterranean University

    lead OTHER

Principal Investigators

  • Aykut Ozçadırcı · Hacettepe University

  • Nur Banu Karaca, MSc. PT. · Hacettepe University

  • Orkun Tüfekçi, MSc. PT. · Hacettepe University

  • Aysima Barlak · Hacettepe University

  • Ali Akdoğan, Prof. Dr. · Hacettepe University

  • Sedat Kiraz, Prof. Dr. · Hacettepe University

  • Edibe Unal, Prof. Dr. · Hacettepe University

  • Sevim Oksüz, PhD. PT. · Eastern Mediterranean University

  • Şule Apraş Bilgen, Prof. Dr. · Hacettepe University

  • Robert D. Gerwin, MD. · Johns Hopkins University

  • Rinnie Geenen, Prof. Dr. · Utrecht University

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-08-01
Primary Completion
2023-08-01
Completion
2023-08-01

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06702839 on ClinicalTrials.gov