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Completed

NCT Number: NCT06738472

Efficacy of Home-Based Posture Exercises as an Addition to Pharmacological Treatment in Fibromyalgia

This interventional study aimed to evaluate the effects of home exercise in addition to pharmacological treatment on pain threshold and spinal mobility in fibromyalgia patients.

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Ahi Evran University

Kırşehir, Turkey (Türkiye)

About this study

Fibromyalgia (FM) is a chronic pain syndrome characterized by widespread musculoskeletal pain, altered pain processing, fatigue, and functional limitations. In addition to pain-related symptoms, individuals with FM frequently present with postural alterations, reduced spinal mobility, and impaired segmental control of the spine, which may contribute to functional disability and reduced quality of life. However, objective assessment of spinal posture and segmental mobility in FM remains limited.

This study aims to comprehensively evaluate spinal posture and sagittal plane mobility in patients with fibromyalgia using the Spinal Mouse®, a validated, non-invasive, computer-assisted device that measures spinal curvature and segmental inclination without radiation exposure. The Spinal Mouse allows for reliable assessment of thoracic and lumbar spinal alignment as well as dynamic movement patterns during functional tasks.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Participants were between the ages of 18 and 65,
  • No diagnosis of rheumatic disease,
  • No diagnosis of chronic comorbid disease,
  • Participants diagnosed with fibromyalgia syndrome according to the European League Against Rheumatism (EULAR) criteria will be included as volunteers.

Exclusion criteria

  • Patients under 18, over 65 years of age
  • Those diagnosed with chronic comorbid diseases
  • Those with a history of rheumatic disease

Treatment and study plan

home based exercises

Other

given exercises to the participants

Primary outcomes

  1. Algometry

    Time frame: 4 weeks

    pain pressure threshold

  2. Spinal mouse for spinal mobility

    Time frame: 4 weeks

    spinal range of motion

Secondary outcomes

  1. Hospital Anxiety and Depression Scale (HADS)

    Time frame: 4 weeks

    used to assess anxiety and depressive symptoms in clinical populations

  2. Pittsburgh Sleep Quality Index (PSQI)

    Time frame: 4 weeks

    Quality of Sleep

  3. Short form-12 (SF-12)

    Time frame: 4 weeks

    Quality of Life

Sponsors and collaborators

Lead sponsor

Kirsehir Ahi Evran Universitesi

Other

Registry information

Important dates

Study start
2025
Primary completion
2025
Study completion
2025
First posted
Dec 17, 2024
Registry last updated
Jan 22, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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