Effects of Soft Tissue Mobilization and Pelvic Floor Muscle Exercises on Pelvic Adhesions

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age40-60
SponsorRiphah International University

About this trial

Adhesions are permanent tissue connections that are created by fibrin deposition between different tissue planes or organs. They are a part of the internal healing process and inflammatory reactions that go through several overlapping phases, including the proliferative phase, remodeling phase, and hemostasis/inflammatory phase. Adhesions are typically the body's defense mechanisms against various triggers of inflammation, including physical, chemical, and infections. These triggers can have unfavorable consequences, including chronic pain, obstruction (particularly bowel), functional impairment, and infertility. This may cause adjacent structures to lose their flexibility and mobility. The nonsurgical treatment of symptoms thought to be associated with adhesions has centered on several methods of soft tissue scar removal.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Married women

Age 40-60 years

BMI below 30 (13)

Women with post-operative pelvic adhesions (14)

Disqualifiers

Women with any other surgery

Women with failed pelvic surgery (14)

Post-operative women with open wound (unhealed suture site) (14)

Women with uncontrolled hypertension, thrombophlebitis, hematoma, osteomyelitis, myositis ossificans and malignancy

Trial design

Design model

Parallel

Treatments tested in this trial

  • soft tissue mobilization with pelvic floor muscle exercises

    Other intervention

    Group A will receive soft tissue mobilization and pelvic floor muscle exercises. Soft tissue mobilization technique will include abdominal myofascial release/trigger point release and deep scar mobilization to decrease pain and improve scar mobility

  • soft tissue mobilization without pelvic floor muscle exercises

    Other intervention

    Group B will receive soft tissue mobilization technique without pelvic floor exercises.

Treatment groups

56 Participants
are divided into 2 treatment groups
Group A: soft tissue mobilization with pelvic floor muscle exercisesExperimental treatment 1 intervention
Group B: soft tissue mobilization without pelvic floor muscle exercisesExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Numeric pain rating scale

The NPRS is a segmented numeric version of the visual analog scale (VAS) in which a respondent selects a whole number (0-10 integers) that best reflects the intensity of his/her pain.

Time frame
6 weeks
2

Female sexual function index

The FSFI questionnaire consists of 19 close-ended questions related to sexual activity and includes six domains: * Sexual desire (question number 1-2) * Sexual arousal (question number 3-6) * Lubrication (question number 7-10) * Orgasm (question number 11-13) * Sexual satisfaction (question number 14-19)

Time frame
6 weeks
3

Functional status questionnaire

The Functional Status Questionnaire (FSQ) is a brief, self-administered questionnaire developed by researchers from Boston's Beth Israel Hospital and the University of California at Los Angeles. The FSQ was designed to screen for disability and to monitor clinically meaningful change in function.

Time frame
6 weeks

Secondary outcomes

Other outcomes

Sponsors and contacts

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