Actively Recruiting

Phase Not Applicable
Age: 20Years - 50Years
All Genders
Healthy Volunteers
ID06835608

Effects of Schroth-Based Three-Dimensional Exercise Program on Angle of Kyphosis, Muscle Strength, Balance, Pain, and Quality of Life in Patients With Postural Hyperkyphosis With Chronic Neck Pain

Led by Baskent University · Updated on 2025-12-03

52

Participants Needed

1

Research Sites

11 weeks

Total Duration

On this page

Sponsors

B

Baskent University

Lead Sponsor

B

Baskent University Ankara Hospital

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are studying the effects of a Schroth-based three-dimensional exercise program on individuals with postural hyperkyphosis and chronic neck pain. This condition involves an increased curvature of the upper spine beyond the normal range, which can negatively impact health, physical performance, and quality of life. The study aims to evaluate how these exercises affect the kyphosis angle, trunk muscle strength, balance, pain, and overall quality of life in affected adults aged 20 to 50 years. Participants will be randomly assigned to one of two groups. The Schroth exercise group will receive electrotherapy to the neck followed by specialized kyphotic posture correction exercises involving spinal lengthening, positional correction, breathing techniques, and neuromuscular re-education. This program will last eight weeks, with 20 sessions over four weeks of combined electrotherapy and exercise, followed by four weeks of exercise alone. The control group will also receive electrotherapy and perform posture corrective exercises focused on strengthening neck and shoulder muscles and stretching tight muscles. Both groups will receive educational sessions on postural awareness and maintain exercise guidance through a brochure. During the study, participants will undergo assessments at baseline, the fourth week, and the eighth week. Measurements will include the thoracic kyphosis angle, trunk muscle strength, balance, spinal stabilization activity, pain intensity, neck disability, and quality of life. The study will monitor these outcomes to understand the impact of the exercise programs on postural kyphosis and chronic neck pain. The total participation time spans eight weeks with regular physiotherapist-led sessions and follow-up evaluations.

CONDITIONS

Brief Title

Effects of Schroth-Based Exercise on Kyphosis Angle, Muscle Strength, Balance, Pain, and Quality of Life in Hyperkyphosis With Chronic Neck Pain

Who Can Participate

Age: 20Years - 50Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Thoracic kyphosis angle greater than 45 degrees
  • Age between 20 and 50 years
  • Neck pain lasting more than 3 months
  • Neck pain visual analogue scale greater than 3
  • No treatment for postural kyphosis in the last 6 months
  • No systemic disease
Not Eligible

You will not qualify if you...

  • History of trauma or surgery on spinal joints
  • Rheumatological or metabolic disorders
  • Congenital postural deformity or scoliosis

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - 8 weeks

Participants receive 20 sessions of electrotherapy and exercise over 4 weeks. After these sessions, exercise sessions continue with a physiotherapist 3 days per week for an additional 4 weeks. The program includes postural education and specific corrective exercises tailored to their group assignment.

20 visits over 4 weeks plus thrice-weekly visits for 4 weeks

Trial Site Locations

Total: 1 location

1

Baskent University Umitkoy Outpatient Clinic

Ankara, Çankaya, Turkey (Türkiye), 06800

Actively Recruiting

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Research Team

T

Tuğçe BAYRAM ERKOYUNCU, PHD Student

H

Hayri Baran YOSMAOĞLU, Proffesor

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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