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The Effects of a Customized Exercise Program on Pain, Kyphosis Angle, and Quality of Life

The Effects of a Customized Exercise Program on Pain, Kyphosis Angle, and Quality of Life in Healthy Adults

Status
Enrolling by invitation
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07477847
Acronym
Exercise
Enrollment
40
Registered
2026-03-17
Start date
2026-03-01
Completion date
2026-04-05
Last updated
2026-03-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Posture

Keywords

kyphosis, exercise, pain, quality of life.

Brief summary

The aim of this study is to evaluate the effect of a customized corrective exercise program on back pain, kyphosis degree, and quality of life in healthy adults. Our hypothesis is that healthy adults participating in a customized exercise program will show a reduction in back pain, a decrease in thoracic kyphosis angle, and an improvement in quality of life in the post-intervention period compared to the control group. The program will continue twice a week for four weeks.

Interventions

OTHERExercise

posture exercises twice a week for four weeks

Sponsors

Istanbul Rumeli University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SEQUENTIAL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Intervention model description

the exercise program

Eligibility

Sex/Gender
ALL
Age
18 Years to 45 Years
Healthy volunteers
Yes

Inclusion criteria

* aged 18-45 years * diagnosed with nonspesific back pain * had not engaged in regular exercise for the past 6 months. * Volunteered to participate

Exclusion criteria

* Individuals with orthopedic problems such as scoliosis or spondylolisthesis, those with acute infections or oncological, neurological, and rheumatological problems, and those already participating in a regular exercise program were excluded.

Design outcomes

Primary

MeasureTime frameDescription
kyphosis indexFrom enrollment to the end of treatment at 4 weeksThe terapist recorded the measurement between c7-T12 with flexiruler
Pain assessmentFrom enrollment to the end of treatment at 4 weeksMc Gill pain Assesment
scapular Protractionfrom enrollment to the end of treatment at 4 weeksThe inferior angle of the scapula was identified by palpation and marked. The horizontal distance between the marked inferior angles of the scapulae was measured using a flexible measuring tape and recorded in centimeters (cm).
Cervical posture0 and 4th weekAnterior neck tilt is recorded.

Secondary

MeasureTime frameDescription
Quality of lifefrom enrollmnent to the end of treatmentSf 36 quality of life survey is recorded.
Trunk flexibility measurementsfrom enrollment to the end of treatment at 4 weeks.Trunk rotation, lateral flexion, and extension measurements are recorded.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 18, 2026