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NCT Number: NCT06907901

Reliability of PHAS in Postural Hyperkyphosis

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.

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Key information

Age range

8 year–65 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Istanbul University-Cerrahpasa

Istanbul, Turkey (Türkiye)

Location status: Recruiting

Location contact

Ayşe Zengin Alpozgen, Assoc. Prof.

CONTACT

[email protected]

05526830479

Kübra Kardeş, Asst. Prof

SUB_INVESTIGATOR

Merve Koyuncu Cenikli, Msc.

SUB_INVESTIGATOR

Selin Uz Tunçay, Msc

SUB_INVESTIGATOR

About this study

This study is designed to assess the reliability of the Postural Habits and Awareness Scale (PHAS) in individuals diagnosed with postural hyperkyphosis. Postural hyperkyphosis is increasingly common due to sedentary lifestyles, prolonged sitting, and technological device use, leading to significant postural deviations and musculoskeletal complaints. Early detection and management of postural habits are essential to prevent long-term spinal deformities and functional limitations.

The PHAS was developed to systematically evaluate individuals' postural awareness and habits in daily life, focusing on factors that contribute to poor posture and spinal alignment. The scale assesses dimensions such as postural habits, awareness of posture-disturbing factors, positional awareness, and ergonomic considerations. However, its psychometric properties, particularly reliability in hyperkyphotic patients, have not yet been established.

This observational, cross-sectional methodological study will employ standardized psychometric methods to analyze the internal consistency and test-retest reliability of the PHAS. The scale's ability to produce stable and consistent results over time will be tested through repeated administration. Additionally, concurrent validity will be examined by comparing PHAS scores with the Kyphosis-Specific Spinal Appearance Questionnaire (KSSA), which measures patients' perception of their spinal deformity.

The findings will provide valuable insights into the scale's utility for clinical and research purposes. Establishing PHAS as a reliable tool could allow physiotherapists, ergonomists, and healthcare professionals to objectively assess postural habits and awareness, design personalized rehabilitation programs, and monitor treatment outcomes. Furthermore, the scale could be integrated into preventive strategies aimed at improving postural control and spinal health in both clinical practice and community settings.

Research Team:

Assoc. Prof. Dr. Ayşe Zengin Alpözgen (Principal Investigator) PhD. PT Kübra Kardeş (Istinye University) MSc PT Selin Uz Tunçay (Istanbul University-Cerrahpasa) MSc PT Merve Koyuncu Cenikli (Istanbul University-Cerrahpasa)

Who can participate

Healthy volunteers accepted: No

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

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

Treatment and study plan

PHAS Assessment

Behavioral

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.

Primary outcomes

  1. Reliability of the Postural Habits and Awareness Scale (PHAS)

    Time frame: 2 weeks

    Internal consistency will be evaluated using Cronbach's Alpha. Test-retest reliability will be assessed by calculating the Intraclass Correlation Coefficient (ICC) between two PHAS administrations. The PHAS consists of 19 items, each scored on a 5-point Likert scale (total score range: 19 to 95). Higher scores indicate better postural habits and awareness. Higher ICC values indicate better reliability.

Secondary outcomes

  1. Kyphosis-Specific Spinal Appearance Questionnaire (KSSAQ)

    Time frame: Baseline

    The KSSAQ is a 10-item, 5-point Likert scale (range: 1 to 5 per item, total score range: 10 to 50) designed to assess patients' perception of their spinal appearance related to thoracic hyperkyphosis. Higher scores indicate worse perceived deformity and greater concern about appearance. The correlation between PHAS and KSSAQ scores will be calculated to determine concurrent validity.

Study contacts

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

Kübra Kardeş, PhD

CONTACT

[email protected]

905387115631

Sponsors and collaborators

Lead sponsor

Istanbul University - Cerrahpasa

Other

Registry information

Official study title

Reliability Analysis of the Postural Habits and Awareness Scale (PHAS) in Patients With Postural Hyperkyphosis

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Apr 2, 2025
Registry last updated
Oct 1, 2025

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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