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Clinical Trials in Turkey / NCT06907901
Recruiting Observational

Reliability of PHAS in Postural Hyperkyphosis

NCT06907901 · tracked via the Priya Life Science Turkey tracker
Phase
Observational
Started
2025-06-01
Last updated
2025-10-01

Condition(s) studied

Postural KyphosisSpineAssessment, Self

Investigational drug(s) / intervention(s)

PHAS Assessment

PHAS Assessment: Participants will complete the Postural Habits and Awareness Scale (PHAS) to assess postural awareness and habits. The scale will be administered twice, two weeks apart, to evaluate reliability.

Study summary

This observational, cross-sectional study aims to evaluate the reliability of the Postural Habits and Awareness Scale (PHAS) in patients with postural hyperkyphosis. The PHAS is designed to assess individuals' postural awareness and habits through four subscales. A total of 128 participants diagnosed with postural hyperkyphosis will complete the PHAS and the Kyphosis-Specific Spinal Appearance Questionnaire (KSSA). Test-retest reliability will be assessed by reapplying the PHAS after two weeks. Internal consistency, test-retest reliability, and concurrent validity will be analyzed. The study aims to provide a valid and reliable tool for evaluating postural awareness in clinical practice and future rehabilitation studies.

Eligibility

Sex
ALL
Min age
8 Years
Max age
65 Years
Healthy volunteers
No
Inclusion Criteria: * Age between 8 and 65 years * Diagnosed with postural hyperkyphosis (Cobb angle ≥ 50° confirmed by clinical and radiological evaluation) * Ability to perform daily activities independently * Voluntary participation and signed informed consent Exclusion Criteria: * Presence of scoliosis or other spinal deformities * Kyphosis due to severe osteoporosis or pathological fractures * Diagnosis of ankylosing spondylitis or other inflammatory spinal diseases * Functional limitations due to acute or chronic pain * Previous postural awareness training or spinal rehabilitation within the last 6 months * Cognitive impairment or severe psychiatric disorder preventing independent questionnaire completion

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Istanbul University-Cerrahpasa Istanbul Istanbul Recruiting

More Istanbul University - Cerrahpasa trials in Turkey

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06907901 on ClinicalTrials.gov ↗ ← All trials in Turkey