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

Investigation of the Effect of Manual Therapy and Pelvic Floor Exercises on Pelvic Floor Muscles in Women With Constipation

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06494917
Enrollment
44
Registered
2024-07-10
Start date
2024-06-14
Completion date
2024-09-30
Last updated
2024-07-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Colonic Inertia, Dyschezia, Constipation

Keywords

constipation, pelvic floor, manual therapy, exercise

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.

Interventions

First arm; Pelvic Floor Exercises (PFE) consisting of diaphragm breathing training, bridge exercise to strengthen the pelvic floor, 3-dimensional diaphragm exercise, 'I Love you massage' for intestinal motility, happy baby pose, child position exercise, full squat, adductor and iliopsoas stretching, mermaid position exercise, 'Shhh' sound exercise, 'Üüüü' sound exercise will be applied.

OTHERPelvic floor exercises and manual therapy techniques

Second arm; Pelvic Floor Exercises (PFE) consisting of diaphragm breathing training, bridge exercise to strengthen the pelvic floor, 3-dimensional diaphragm exercise, 'I Love you massage' for intestinal motility, happy baby pose, child position exercise, full squat, adductor and iliopsoas stretching, mermaid position exercise, 'Shhh' sound exercise, 'Üüüü' sound exercise will be applied. In addition to diaphragmatic breathing training and pelvic floor exercises, manual therapy methods such as momentum minus mobilisation, sphincter opening, colon massage, global fascia manipulation, trigger point and myofascial release will be applied.

Sponsors

Istanbul Arel University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 55 Years
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
Constipation Quality of Life questionnairewill be evaluated at the first session and at the end of session 6evaluates 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

MeasureTime frameDescription
Constipation Severity Scalewill be evaluated at the first session and at the end of session 6scale 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.

Other

MeasureTime frameDescription
Bristol stool chartwill be evaluated at the first session and at the end of session 6Bristol stool chart is a medical aid designed to classify faeces into seven groups.
Rome IV Criteriawill be evaluated at the first session and at the end of session 6categorizes disorders of chronic constipation into four subtypes: (a) functional constipation, (b) irritable bowel syndrome with constipation, (c) opioid-induced constipation, and (d) functional defecation disorders, including inadequate defecatory propulsion and dyssynergic defecation
bowel diaryDuring the 6-week studya record you keep of when and how much faeces (poo) you passed or leaked during the day and overnight.

Countries

Turkey (Türkiye)

Contacts

Primary Contactislek
cihanislek97@gmail.com+905442755137
Backup ContactHalis Doğan, phd
halisdogan@arel.edu.tr+90532 200 08 43

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026