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Investigation of the Effect of Manual Therapy and Pelvic Floor Exercises on Pelvic Floor Muscles

Not Applicable
Recruiting
Conditions
Dyschezia
Colonic Inertia
Constipation
Interventions
Other: pelvic floor exercises
Other: Pelvic floor exercises and manual therapy techniques
Registration Number
NCT06494917
Lead Sponsor
Istanbul Arel University
Brief Summary

The goal of this clinical trial is to Investigation of the effect of manual therapy and pelvic floor exercises on pelvic floor muscle in women with constipation. The main question\[s\] it aims to answer are:

* In addition to pelvic floor exercises, manual therapy applied to the pelvic floor muscles has no impact on constipation.

* In addition to pelvic floor exercises, manual therapy applied to the pelvic floor muscles has an impact on constipation.

Participants will apply pelvic floor exercises and manual therapy techniques. If there is a comparison group: Researchers will compare \[insert groups\] to see if \[insert effects\].

Detailed Description

* Female participants aged 18-55 years with constipation complaints will be recruited through social media and hospital outpatient clinics, and those who volunteer to participate will be enrolled in the study.

* Participants will be assessed as group 1 (pelvic floor exercises), group 2 (pelvic floor exercises + manual therapy techniques). Group 1 will receive diaphragmatic breathing training and then pelvic floor exercises to strengthen the pelvic floor.

* Group 2 will receive manual therapy methods consisting of Momentum Minus Mobilisation, Sphincter Opening, Colon Massage, Global Fascial Manipulation, Trigger Point and Myofascial Release in addition to Diaphragmatic Breathing Training and Pelvic Floor Exercises.

* Participants will receive exercise training 5 days a week for 6 weeks. Manual therapy methods will be used 2 days a week for the first 2 weeks and then 1 day a week. Initial assessment of participants and manual therapy applications will be done face to face. The exercises will be continued using the online telerehabilitation method.

* Both groups will be given nutritional advice, such as drinking plenty of water, eating fibre-rich foods and preferring foods that aid digestion. Participants will be advised to take their time every day, in the morning, at the same time, without rushing to defecate, preferring an squat toilet, which increases intra-abdominal pressure, half an hour after meals, but not for more than five minutes.If a European toilet is used, toilet training will be given about leaving a 15-18 cm long ridge under the feet.

* Both groups will be given assessment tests before and at the end of the trial and the results will be compared.

Recruitment & Eligibility

Status
RECRUITING
Sex
Female
Target Recruitment
44
Inclusion Criteria
  • Constipation in the last 6 months
  • Being able to use smartphones and social media (whatsapp and instagram)
  • Not having a health problem that prevents exercise
  • Able to communicate
  • Literate
Exclusion Criteria
  • Not had constipation in the last 6 months
  • Pregnancy or recent pregnancy
  • had surgery
  • having a tumour
  • Having vertigo Taking medication (use of bowel-regulating drugs)
  • Previous physiotherapy for constipation problems
  • Inflammatory bowel disease

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
pelvic floor exercisespelvic floor exercisesDiaphragmatic breathing training and Pelvic Floor Exercises will be applied.Participants will receive exercise training 5 days a week for 6 weeks.
Pelvic floor exercises and manual therapy techniquesPelvic floor exercises and manual therapy techniquesIn addition to diaphragmatic breathing training and pelvic floor exercises, manual therapy methods will be applied. Participants will receive exercise training 5 days a week for 6 weeks. Manual therapy methods will be used 2 days a week for the first 2 weeks and then 1 day a week.
Primary Outcome Measures
NameTimeMethod
Constipation Quality of Life questionnairewill be evaluated at the first session and at the end of session 6

evaluates constipation through daily individual health assessment and functioning. The highest score that can be obtained from the scale is 140 and the lowest score is 28. It is thought that quality of life is negatively affected as scores on the scale increase.

Secondary Outcome Measures
NameTimeMethod
Constipation Severity Scalewill be evaluated at the first session and at the end of session 6

scale that is calculated as a sum of a 5-point ordinal frequency ratings for the six Rome III (IV) functional constipation questions. The lowest score is 0 and the highest is 73. A high score on the scale indicates that the symptoms are at a severe level.

Trial Locations

Locations (1)

Cizre Dr Selahattin Cizrelioglu State Hospital

🇹🇷

Şırnak, Turkey

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