Actively Recruiting

Phase Not Applicable
Age: 18Years - 60Years
FEMALE
NCT05978414

Functional Links Between the Temporomandibular Joint and the Pelvis in Gynecology

Led by Poznan University of Physical Education · Updated on 2025-02-07

200

Participants Needed

1

Research Sites

146 weeks

Total Duration

On this page

Sponsors

P

Poznan University of Physical Education

Lead Sponsor

U

University of Life Science in Poznan

Collaborating Sponsor

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

Functional Links Between the Temporomandibular Joint and the Pelvis in Gynecology

Who Can Participate

Age: 18Years - 60Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Written consent to participate in the study
  • Female patients after surgical treatment for genital prolapse or diagnosed endometriosis
Not Eligible

You will not qualify if you...

  • No written consent to participate in the study
  • Cancer
  • Injury to the temporomandibular joint and pelvis
  • Fibromyalgia
  • Rheumatic diseases
  • Withdrawal of participation at any stage of the study

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Poznan University of Physical Education

Poznan, Poland, 61-871

Actively Recruiting

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Research Team

M

Małgorzata E Wójcik, Dr

CONTACT

A

Anna M Paczkowska, Dr

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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