Comparison of Two Different Pelvic Floor Muscle Training Programs in Stress Urinary Incontinence

Sponsor
Hacettepe University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05293886
Collaborator
(none)
44
1
2
18.5
2.4

Study Details

Study Description

Brief Summary

Pelvic floor muscle training (PFMT) is indicated as a first-line treatment for stress urinary incontinence. PFMT aims to improve pelvic floor muscle strength, endurance and relaxation ability or a combination of these. PFMT is a structured and customized exercise program. Pelvic floor muscles work in synchronization with many muscles and pelvic floor muscle function is supported by synergistic muscles. Relationships between the functions of pelvic floor muscles and synergistic muscle groups have been reported in the literature. However, studies comparing the efficacy of PFMT and combined training of these muscles are limited and more studies are needed.

Therefore the aim of this study is to compare the effects of isolated PFMT and functional PFMT in women with stress urinary incontinence.

Condition or Disease Intervention/Treatment Phase
  • Other: Classical Pelvic Floor Muscle Training
  • Other: Functional Pelvic Floor Muscle Training
N/A

Detailed Description

Our study is designed as a parallel group, randomized clinical trial. Participants who meet the inclusion criteria will be assigned randomly to one of the study groups. The participants in the 1st group will be given classical PFMT, and the participants in the 2nd group will be given functional PFMT. The study period is 8 weeks for each individual participating in the study. All participants will be called for control every 2 weeks and progress will be made in exercise programs in accordance with the protocol.

At the beginning of the study, demographic informations, physical characteristics, smoking habit, primary and secondary urinary symptoms and their duration, obstetric history, menstrual and menopausal status, comorbidities, drugs used and, if any, the effects of these drugs on the urinary system, previous UI treatments and their duration will be recorded.

For individuals over 65 years of age, Mini Mental Test will be applied in terms of cooperation suitability for the research.

The objective severity of incontinence will be assessed with the 1-hour pad test. The subjective severity of incontinence and its impact on life will be evaluated with the International Incontinence Consultation Questionnaire-Short Form (ICIQ-UI SF). The King's Health Questionnaire (KHQ) will be used to investigate the effects of interventions on the sub-dimensions of quality of life. With the Patient Global Impression of Severity Scale and the Patient Global Impression of Change Scale, the individual's perception of severity and recovery of UI will be evaluated. Vaginal palpation will be performed to determine whether individuals can voluntarily contract their pelvic floor muscles and to teach correct contraction before pelvic floor muscle training. Outcome measurements will be recorded at the beginning of the study, at the end of the 4th week and at the end of the 8th week. Participants will be given an exercise diary to increase motivation and exercise adherence.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
44 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Comparison of The Effects of Two Different Pelvic Floor Muscle Training Programs in Women With Stress Urinary İncontinence
Anticipated Study Start Date :
Apr 15, 2022
Anticipated Primary Completion Date :
Oct 30, 2023
Anticipated Study Completion Date :
Oct 30, 2023

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Classical Pelvic Floor Muscle Training

In the first 2 weeks of classical pelvic floor muscle training, individuals will perform 3 sets of 10 maximal voluntary pelvic floor muscle contraction exercises and 20 submaximal voluntary pelvic floor muscle contraction exercises per day. In every 2-week control, the number of sets will be increased by one set.

Other: Classical Pelvic Floor Muscle Training
In the first 2 weeks of classical pelvic floor muscle training, individuals will perform 3 sets of 10 maximal voluntary pelvic floor muscle contraction exercises and 20 submaximal voluntary pelvic floor muscle contraction exercises per day. In every 2-week control, the number of sets will be increased by one set.

Experimental: Functional Pelvic Floor Muscle Training

Functional pelvic floor muscle training will be started with 3 exercises (toe tap, bridge and clamshall exercises), each exercise will be performed with 1 set and 30 repetitions. In every 2-week control, the number of exercises will be increased by one. Cat-cow exercise will be added at 3-4th weeks, squats will be added at 5-6th weeks, and lunges will be added at 7-8th weeks.

Other: Functional Pelvic Floor Muscle Training
Functional pelvic floor muscle training will be started with 3 exercises (toe tap, bridge and clamshall exercises), each exercise will be performed with 1 set and 30 repetitions. In every 2-week control, the number of exercises will be increased by one. Cat-cow exercise will be added at 3-4th weeks, squats will be added at 5-6th weeks, and lunges will be added at 7-8th weeks.

Outcome Measures

Primary Outcome Measures

  1. Change in Symptom Severity and Impact of Incontinence on Life [Change in International Urinary Incontinence Consultation Questionnaire Short Form score from baseline to end of 8th week]

    International Urinary Incontinence Consultation Questionnaire Short Form (ICIQ-UI SF) will be used to evaluate the change in symptom severity and impact of incontinence on life

Secondary Outcome Measures

  1. Incontinence Severity [Change in incontinence severity from baseline to end of 8th week]

    1-hour pad test will be used to evaluate the incontinence severity

  2. The Impact of Incontinence on Quality of Life [Change in King Health Questionnaire score from baseline to end of 8th week]

    King Health Questionnaire will be used to evaluate the effect of incontinence on quality of life

  3. Participant's Perception of Symptom Severity [Change in Patient Global Impression of Severity Scale score from baseline to end of 8th week]

    Patient Global Impression of Severity Scale will be used to evaluate the participant's perception of symptom severity

  4. Participant's Perception of Recovery [Change in Patient Global Impression of Change Scale score from baseline to end of 8th week]

    Patient Global Impression of Change Scale will be used to evaluate the participant's perception of recovery

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patients suffering from stress urinary incontinence or SUI predominant Mixed Urinary Incontinence according to the 3 Incontinence Questionnaire (3IQ)

  • Body mass index <35 kg/m²

  • Individuals over the age of 18 (with a Mini Mental Test score ≥ 24 for individuals over the age of 65)

Exclusion Criteria:
  • Patients with pure urge incontinence, urge predominant mixed urinary incontinence or neurogenic bladder

  • Pregnancy or suspected of pregnancy

  • Those who have given birth in the last 1 year

  • Being virgin

  • Those who have had abdomino-pelvic surgery in the last 6 months, and/or those who have received abdomino-pelvic radiotherapy

  • Those with urinary tract infection, recurrent urinary tract infection, diagnosis of interstitial cystitis

  • Any orthopedic problem that will hinder exercise

  • Patients over 65 years of age with a mini mental test score < 24

  • Patients with Pelvic Organ Prolapse grade ≥ Stage 2

  • Those who have received treatment for urinary incontinence in the last 6 months

  • Those who have uncontrolled diabetes and hypertension, severe systemic disease

  • Those who have a neurological disease that will affect the urinary system

  • Those who have started a new drug that will affect bladder functions in the last 1 month

  • The strength of the pelvic floor muscles in digital examination is <2 according to the Modified Oxford Scale score.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Berna Tokmak Ankara Turkey 06100

Sponsors and Collaborators

  • Hacettepe University

Investigators

  • Principal Investigator: Serap Özgül, Assoc Prof, Hacettepe University

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
SERAP ÖZGÜL, Doc. Dr., Hacettepe University
ClinicalTrials.gov Identifier:
NCT05293886
Other Study ID Numbers:
  • KA-21107
First Posted:
Mar 24, 2022
Last Update Posted:
Mar 24, 2022
Last Verified:
Mar 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 24, 2022