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Clinical Trial Summary

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.


Clinical Trial Description

Methods After taking a detailed history, patients will be asked to: 1. Completing: the SF-36 quality of life assessment questionnaire and Female Sexual Function Index assessment, and marking on a numerical scale their pain sensations for the temporomandibular joint and for the pelvis. The SF-36 questionnaire, FSFI scale, and numerical scale (assessing pain sensations for the temporomandibular joint and pelvic joint), will also be subjected to completion/checking after the completion of manual visceral treatments in groups with physiotherapy intervention for both conditions. 2. Type of postural pattern according to Hall-Wernham-Littlejohn: type I - normal, type II - anterior pelvic tilt, type III - posterior pelvic tilt. 3 Pelvic type assessment: normal, high, low; pelvic type will be assessed in each patient and in groups with physiotherapeutic intervention for both conditions before and after manual visceral treatments. 4. Assessment of mobility in the temporomandibular joints in the sagittal plane CromWell digital caliper, and diagnosis using standardized protocols. 5. Postural assessment on the Posturomed Technomex platform and Podoscope Sensor Medica. 6. 6.Manual visceral treatments The treatments will be performed after the patient is qualified by the obstetrician-gynecologist specialist. 7. After performing techniques and placebo in both groups, filling out questionnaires again, measuring on the platform, pattern posture.. 8. Statistical analysis: upon completion of the study, the collected quantitative and qualitative data will be subjected to statistical analysis. The choice of statistical tools will depend on the obtained probability distribution. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05978414
Study type Interventional
Source Poznan University of Physical Education
Contact Malgorzata E Wójcik, Dr
Phone +4895 727 91 00
Email m.wojcik@awf-gorzow.edu.pl
Status Recruiting
Phase N/A
Start date November 14, 2023
Completion date September 1, 2026

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