An interventional study of Exercise in Posture, sponsored by Istanbul Rumeli University. Enrolling by invitation at 1 site in Turkey (Türkiye). Open to participants aged 18 Years to 45 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-03-17.
Sponsored by Istanbul Rumeli University · Not applicable, Interventional, and Treatment
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.
132 studies on the registry are indexed under Kyphosis; 31 are open to participants now.
This study's planned enrollment of 40 is close to the median of 44 across 82 interventional studies indexed under Kyphosis.
Browse Kyphosis studies →Istanbul Rumeli University is the lead sponsor of 26 studies on the registry; 11 are open to participants now.
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Exclusion Criteria:
posture exercises twice a week for four weeks
kyphosis index
The terapist recorded the measurement between c7-T12 with flexiruler
Time frame: From enrollment to the end of treatment at 4 weeks
Pain assessment
Mc Gill pain Assesment
Time frame: From enrollment to the end of treatment at 4 weeks
scapular Protraction
The 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).
Time frame: from enrollment to the end of treatment at 4 weeks
Cervical posture
Anterior neck tilt is recorded.
Time frame: 0 and 4th week
Quality of life
Sf 36 quality of life survey is recorded.
Time frame: from enrollmnent to the end of treatment
Trunk flexibility measurements
Trunk rotation, lateral flexion, and extension measurements are recorded.
Time frame: from enrollment to the end of treatment at 4 weeks.
PDFs hosted by the registry, ClinicalTrials.gov.
Ran from Mar 2026 to primary completion in Mar 2026, 0 months.
Of 56 non-industry interventional studies with no phase under Kyphosis, half reached primary completion within 9 months of starting (the median), counting those still running; a quarter within 4 and three quarters within 30. This study's 0 months is below that.
Counting every sponsor, half of 58 studies reached it within 9 months; a quarter within 4 and three quarters within 30.
How these figures are worked out, and which studies are left out of them.
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Istanbul Rumeli University