Viewing Study NCT07447193


Ignite Creation Date: 2026-03-26 @ 3:18 PM
Ignite Modification Date: 2026-03-31 @ 1:47 AM
Study NCT ID: NCT07447193
Status: NOT_YET_RECRUITING
Last Update Posted: 2026-03-03
First Post: 2026-02-25
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: Investigation of Pain Perception According to Gender in Individuals With Scoliosis
Sponsor: Uskudar University
Organization:

Study Overview

Official Title: Investigation of Pain Perception According to Gender in Individuals With Scoliosis
Status: NOT_YET_RECRUITING
Status Verified Date: 2026-02
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: 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.
Detailed Description: 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).

Study Oversight

Has Oversight DMC: False
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: