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Visceral Osteopathic Manual Therapy Methods in Women With Stress Urinary Incontinence

I

Istanbul Rumeli University

Status

Not yet enrolling

Conditions

Osteopathic Manipulative Treatment (OMT)

Treatments

Other: visceral osteopathic manual therapy

Study type

Interventional

Funder types

Other

Identifiers

NCT06874543
IRU-FTR-NA-01

Details and patient eligibility

About

The aim of this study is to evaluate the effect of visceral osteopathic manual therapy method for stress urinary incontinence in female patients. As a result of the study, the effect of visceral osteopathic manual therapy fascial release on bladder control, quality of life and flexibility will be evaluated.

Full description

Urinary incontinence (UI) is an important health problem that occurs when continence cannot be achieved and negatively affects the lives of individuals according to the International Continence Society (ICS). Stress urinary incontinence (SUI), one of the most common types of UI, is a problem that occurs during coughing, laughing, sneezing, exercise (one of which is caused by increased intra-abdominal pressure (Valsalva maneuver) and shows a steady increase in women with age. The aim in the treatment of SUI is to ensure that patients regain their continence skills. In recent years, conservative treatment methods have been preferred more in the treatment of SUI due to their ease of application and low cost. It is thought that Osteopathic Manual Therapy (OMT) reduces the negative effects of musculoskeletal pain and dysfunction on body systems, improves respiratory mechanics, venous and lymphatic drainage, and accordingly supports homeostasis and optimizes functions.

In this study, it is planned to investigate the effect of the visceral system and visceral fascia on SUI.

It is thought that the fascia surrounding the internal organs can be loosened and systematic diseases can be affected with the visceral osteopathic manual therapy (VOMT) method, which is among the osteopathic manual therapy methods.

Within the scope of the study, 40 volunteer female patients diagnosed with SUI will be evaluated and randomly divided into 2 groups. Day 1 evaluation scales will be applied to both groups, VOMT methods will be applied to the experimental group a total of four times a week, and bladder mobilization will be given as a home program, and no application will be made to the control group. Both groups will be re-evaluated in months 1 and 4. The inadequacy of studies conducted on this subject was an important factor in choosing this method.

Enrollment

40 estimated patients

Sex

Female

Ages

18 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Being a woman between the ages of 18 and 70
  • Being able to communicate in Turkish
  • Being able to read and write
  • Being able to understand and follow verbal prompts
  • Being willing to participate in the study

Exclusion criteria

  • Pregnancy
  • Presence of prolapse
  • Presence of vaginal and urinary system infection or malignancy
  • Presence of neurological damage
  • Having had any disease that may cause incontinence
  • Having had surgery for SUI or urogynecological reasons in the last 2 months.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

40 participants in 2 patient groups

Group 1: Study group visceral osteopathic manual therapy method will be applied
Active Comparator group
Description:
In the study, relaxation techniques, hepato-gastric ligamentum mobilization, pyloric valve mobilization, sphincter odi mobilization, sphincter ilio-jejunum mobilization, cecal valve mobilization, iliopsoas and iliacus mobilization, peritoneal mobilization, intestine, kidney, bladder, stomach, liver and bladder organ mobilizations will be applied to the experimental group patients as VOMT program. Until the next session, bladder mobilization will be taught as a home program and they will be asked to do it every day. After VOMT is applied by the physiotherapist once a week, a total of 4 times, the evaluation scales will be applied again. In order to see the long-term effect, the patients will be evaluated again in the first month and the third month after the end of the treatment. The forms will be filed as pre-treatment, post-treatment, first month and third month data and will be entered into the computer and recorded.
Treatment:
Other: visceral osteopathic manual therapy
Group 2: Evaluation scales will be applied to control group patients on the first day, and the scale
No Intervention group
Description:
They were evaluated on the first application day and followed up ten times in parallel with the study group, at 1 month, 2 months and 4 months, a total of 4 times.

Trial contacts and locations

1

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Central trial contact

ALİ CIMBIZ, PROFESSOR; NEZAHAT AKIN, PHSİOTHERAPİST

Data sourced from clinicaltrials.gov

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