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NCT Number: NCT07447193

Investigation of Pain Perception According to Gender in Individuals With Scoliosis

The aim of this study is to evaluate whether pain perception under spinal pressure created on a physiotherapy roller differs according to gender in individuals diagnosed with scoliosis.

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Key information

Age range

18 year–45 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Badam Medical Center

Baku, Azerbaijan

Location status: Recruiting

Location contact

Aynur SHIRALIZADA

CONTACT

About this study

This study will be conducted using a single-group pre-test-post-test quasi-experimental design. Participants will undergo sports physiotherapy-based exercises designed to create controlled mechanical pressure on the spine using a physiotherapy roller. The aim of the exercises is to evaluate the changes in pain perception during the pressure created on the spinal infrastructure and the postural control mechanisms specific to scoliosis, and whether these changes differ according to gender. The exercise program will be applied three days a week for a total of six weeks, with each exercise session lasting approximately 45 minutes. All applications will be performed under the supervision of a physiotherapist, and the spinal pressure created on the physiotherapy roller during the exercises will be controlled and within the limits that individuals can tolerate. The physiotherapy roller will be used as the main equipment in this study, not as an auxiliary tool, and will ensure that spinal pressure is created in a standard manner. Pain assessment will be conducted in two stages: before the exercise program (pre-test) and after the exercise program is completed (post-test).

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Having a clinical or radiological diagnosis of scoliosis
  • Being between 18-45 years of age
  • Not having undergone scoliosis surgery in the last 6 months
  • Agreeing to participate in the study voluntarily

Exclusion criteria

  • Having a history of neurological disease
  • Acute inflammatory spinal disease
  • Serious cardiovascular or systemic diseases that would prevent participation in exercise

Treatment and study plan

Exercise

Other

The exercise program will be implemented three days a week for a total of six weeks, with each exercise session planned to be approximately 45 minutes long. All applications will be carried out under the supervision of a physiotherapist, and the spinal pressure created on the physiotherapy cylinder during the exercises will be controlled and applied within the limits that individuals can tolerate. The physiotherapy cylinder will be used as the main equipment, not an auxiliary one, in this study and will ensure that spinal pressure is created in a standard manner.

Primary outcomes

  1. Scoliosis Research Society-22

    Time frame: 8 weeks

    Scoliosis Research Society-22 is a functional survey for the patient to fill out on their scoliosis. This survey has been validated in the literature. It is a 22 question survey on the functional status and pain that a patient experiences. Created by the scoliosis research society. There is a scoring rubric that goes with the survey. This survey has 5 domains that are covered with the minimum score of 22 and the maximum score of 110. The higher the score the better the patient is doing in the domains of: Activities of Daily Living, Mental Health, Pain, Patient Satisfaction, Positive Affect, Quality of Life, Social Relationships, and Stress/Coping.

Study contacts

Contact information is provided by the study sponsor or research team.

Ömer ŞEVGİN

CONTACT

[email protected]

+905069787535

Sponsors and collaborators

Lead sponsor

Uskudar University

Other

Registry information

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Mar 3, 2026
Registry last updated
Apr 9, 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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