About this trial
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.
Eligibility criteria
Qualifiers
Written consent to participate in the study.
Female patients after surgical treatment with prolapse of reproductive organs and diagnosed endometriosis.
Disqualifiers
No written consent to participate in the study.
Cancer.
Injury to the temporomandibular joint and pelvis.
Fibromyalgia.
Trial design
Treatments tested in this trial
- Visceral therapy
- Placebo
Treatment groups
Sponsors and collaborators
Poznan University of Physical Education
Lead sponsor
University of Life Science in Poznan
Collaborator