Condition: Prolapse; Female · Endometriosis-related Pain · Sponsor: Poznan University of Physical Education
1 Recruitment. 2. Collection of written consents for the study. 3. Random assignment to groups with and without intervention. 4. Completion of questionnaires by study participants, postural pattern assessment, temporomandibular joint assessment, and platform assessment. 5\. Performance of visceral therapy in the group with intervention, in the group without intervention placebo. Duration 5 weeks, treatment 1x per week at the same time of day and given day e.g. Mondays only. 6\. Reassessment as in step 4. 7. Data collection, statistical analyses. 8. Interpretation of results for female participants. 9. Preparation of results for scientific publications.
This description comes directly from the study's public registry record.
Małgorzata E Wójcik, Dr · +4895 727 91 00 · m.wojcik@awf-gorzow.edu.pl
Anna M Paczkowska, Dr · +4861 285 40 31
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| Poznan University of Physical Education | Poznan, Poland | Recruiting |
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Source record: clinicaltrials.gov/study/NCT05978414