NCT07598591

Brief Summary

This study is designed as a randomized controlled trial to evaluate the additional benefits of Basic Body Awareness Therapy (BBAT) when combined with a corrective exercise program for adolescents with postural hyperkyphosis. Postural hyperkyphosis, defined as a thoracic kyphosis angle of 40 degrees or greater, often leads to physical misalignments and psychosocial issues such as decreased self-esteem and poor body image during adolescence. Participants will be randomly assigned to either Group A (Experimental) or Group B (Control) using a stratified block randomization method. Both groups will participate in a 12-week intervention consisting of supervised Schroth corrective exercises performed twice weekly. Group A will additionally receive one session per week of BBAT, a physiotherapy method focusing on movement quality, mental awareness, and the integration of physical and mental self-awareness through lying, sitting, standing, and walking exercises. Group B will receive Autogenic Training, a systematic relaxation technique, as an active control. Assessments will be conducted at baseline and at the end of the 12-week program. The primary outcome measures include body awareness (Body Awareness Questionnaire), aesthetic perception of the spine (Kyphosis Specific Spinal Appearance Questionnaire), self-esteem (Rosenberg Self-Esteem Scale), and digital posture analysis (PostureScreen Mobile). Secondary outcomes involve clinical measurements of kyphosis (Flexicurve and Wall-Occiput Distance), dynamic and static balance (Y-Balance Test and Single-Leg Stance Test), thoracic joint position sense, health-related quality of life (SRS-30), and pain intensity (Numeric Pain Rating Scale). The study aims to provide a comprehensive understanding of how mindfulness and movement awareness can enhance traditional physical rehabilitation for spinal postural disorders.

Trial Health

63
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
60

participants targeted

Target at P25-P50 for not_applicable

Timeline
14mo left

Started May 2026

Geographic Reach
1 country

1 active site

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

May 14, 2026

Completed
6 days until next milestone

First Posted

Study publicly available on registry

May 20, 2026

Completed
9 days until next milestone

Study Start

First participant enrolled

May 29, 2026

Expected
1 year until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 29, 2027

2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

July 29, 2027

Last Updated

May 20, 2026

Status Verified

May 1, 2026

Enrollment Period

1 year

First QC Date

May 14, 2026

Last Update Submit

May 14, 2026

Conditions

Keywords

Postural HyperkyphosisBasic Body Awareness TherapyCorrective ExerciseAdolescent PostureBody ImageSelf-EsteemSchroth MethodMind-Body InterventionSpinal DeformityExercise Therapy

Outcome Measures

Primary Outcomes (4)

  • Body Awareness - Body Awareness Questionnaire (BAQ)

    The Body Awareness Questionnaire is an 18-item scale designed to assess a person's sensitivity to non-pathological bodily processes, such as body rhythms and changes in bodily states. Each item is rated on a 7-point Likert scale, with total scores ranging from 18 to 126. A higher total score indicates a greater level of body awareness. This measure will evaluate how the interventions influence the participants' internal perception of their bodies.

    12 weeks

  • Aesthetic Perception of the Spine - Kyphosis Specific Spinal Appearance Questionnaire (KSAQ)

    The Kyphosis Specific Spinal Appearance Questionnaire consists of 22 items specifically tailored to evaluate how adolescents with hyperkyphosis perceive the aesthetic appearance of their spine. The scale uses a 5-point Likert system where higher scores reflect a more negative perception of spinal appearance and higher treatment expectations. This tool provides insight into the psychosocial impact of postural changes and the perceived effectiveness of the treatment from the patient's perspective.

    12 weeks

  • Self-Esteem - Rosenberg Self-Esteem Scale (RSES)

    The Rosenberg Self-Esteem Scale is a widely validated 10-item instrument used to measure global self-worth and self-acceptance. Participants rate each item on a 4-point Likert scale ranging from strongly agree to strongly disagree. It captures both positive and negative feelings about the self, providing a total score that reflects the individual's overall level of self-esteem throughout the therapeutic process.

    12 weeks

  • Posture Analysis - PostureScreen Mobile (PSM) Assessment

    PostureScreen Mobile is a digital postural analysis application used to objectively quantify postural deviations. It measures shifts and tilts in centimeters or degrees by analyzing photos taken from anterior, posterior, and lateral views. The assessment focuses on identifying improvements in spinal alignment and the reduction of forward head posture or thoracic kyphosis after the 12-week intervention.

    12 weeks

Secondary Outcomes (8)

  • Thoracic Kyphosis Angle Measured by Flexicurve

    12 weeks

  • Wall-Occiput Distance (WOD)

    12 weeks

  • Y-Balance Test (YBT)

    12 weeks

  • Single-Leg Stance Test (SLS)

    12 weeks

  • Joint Position Sense

    12 weeks

  • +3 more secondary outcomes

Study Arms (2)

Group A

EXPERIMENTAL

Participants in Group A will receive a multimodal program combining Schroth-based corrective exercises and Basic Body Awareness Therapy (BBAT). The intervention includes posture-focused Schroth movements and BBAT elements such as body scanning, breathing awareness, and center-of-line stimulation. The intervention will be delivered twice weekly over 12 weeks, with an additional weekly group BBAT session, totaling 36 supervised 60-minute sessions by a certified physiotherapist

Other: Corrective Exercise and Basic Body Awareness Therapy (BBAT)

Group B

ACTIVE COMPARATOR

Participants in Group B will receive a program combining Schroth-based corrective exercises and Autogenic Training. Corrective exercises will be performed with the same intensity and frequency as Group A, adjusted to individual tolerance. Autogenic Training includes self-suggestion formulas for deep relaxation, focusing on sensations of heaviness and warmth. The intervention will be delivered twice weekly over 12 weeks, totaling 24 supervised 60-minute sessions by a physiotherapist.

Other: Corrective Exercise and Autogenic Training

Interventions

This is a behavioral, non-drug intervention combining Schroth corrective exercises with somatic awareness through Basic Body Awareness Therapy (BBAT). Movements emphasize movement quality, postural alignment, and improved self-perception of the body. The approach supports individualized progression (targeting 4-6 on a perceived difficulty scale) and complements conventional physiotherapy for adolescent hyperkyphosis.

Group A

This is a non-drug corrective exercise program tailored for adolescents with postural hyperkyphosis, combined with Autogenic Training for relaxation. It includes spinal strengthening and Schroth-specific postural corrections performed twice weekly. Additionally, participants perform Autogenic Training focusing on breathing, cardiac regulation, and abdominal warmth to support mental well-being alongside physical rehabilitation.

Group B

Eligibility Criteria

Age10 Years - 18 Years
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64)

You may qualify if:

  • Adolescents aged between 10 and 18 years.
  • Diagnosis of postural hyperkyphosis confirmed by a thoracic kyphosis angle of 40 degrees or greater.

You may not qualify if:

  • Diagnosis of congenital or rigid spinal deformities, such as Scheuermann's kyphosis.
  • History of major spinal surgery, severe spinal trauma, or significant orthopedic conditions.
  • Presence of diagnosed neurological or vestibular diseases that may affect balance or movement.
  • Use of spinal braces or other corrective orthotic devices during the study period.
  • Having received formal physiotherapy or a structured exercise program for posture within the last 6 months.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Istanbul University-Cerrahpaşa

Istanbul, 34500, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Scheuermann Disease

Interventions

Autogenic Training

Condition Hierarchy (Ancestors)

Spinal OsteochondrosisOsteochondrosisBone DiseasesMusculoskeletal DiseasesKyphosisSpinal CurvaturesSpinal Diseases

Intervention Hierarchy (Ancestors)

HypnosisMind-Body TherapiesComplementary TherapiesTherapeuticsPsychotherapyBehavioral Disciplines and Activities

Study Officials

  • Ayşe Zengin Alpözgen, Assoc Prof.

    Istanbul University - Cerrahpasa

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Aslı YILDIRIM HAKANER

CONTACT

Ayşe Zengin Alpözgen, Assoc. Prof.

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Associate Professor

Study Record Dates

First Submitted

May 14, 2026

First Posted

May 20, 2026

Study Start (Estimated)

May 29, 2026

Primary Completion (Estimated)

May 29, 2027

Study Completion (Estimated)

July 29, 2027

Last Updated

May 20, 2026

Record last verified: 2026-05

Data Sharing

IPD Sharing
Will not share

Locations