Effectiveness of Modern Physical Agents in the Treatment of Pelvic Floor Dysfunctions
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: modern agents rehab, classical rehab.
- Who it may be relevant to
- Registry conditions: Pelvic Floor Dysfunctions. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Lithuania
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
The Effectiveness of Modern Physical Agents in Treating Pelvic Floor Dysfunctions, Improving Functional State, Life Quality, and Biosocial Functions During First-stage Pelvic Rehabilitation.
Overview
This clinical trial aims to determine whether adding modern physical agents (high-intensity laser therapy, magnetotherapy, radial shock wave therapy, kinesiotaping) in conjunction with classical rehabilitation interventions produces superior outcomes in treating pelvic floor dysfunction compared to classical rehabilitation interventions alone. It will also assess the safety of these agents in the context of pelvic floor dysfunction rehabilitation. The main questions it aims to answer are: Does adding modern physical agents to the treatment of pelvic floor dysfunction improve symptoms, impairments in functional state, quality of life, and biosocial functions more effectively than classical interventions alone? Participants who experience pelvic floor dysfunction during primary rehabilitation will receive: Either an individualized rehabilitation intervention plan comprising 20 classical procedures in combination with modern physical agents or classical interventions alone. Rehabilitation will take place in the outpatient rehabilitation department. Patients will visit the clinic for a comprehensive functional state assessment and then for individualized procedures; the entire plan will be delivered over three months, after which participants will return for follow-up checkups and assessments after the procedures and again after six months.
Detailed description
After subjects are included in the research, two groups (interventional-modern agents rehab and control-classical rehab) of 125 patients each will be formed through concealed randomization. A person not connected with the study will use a random number generator to allocate subjects to the groups.
The rehabilitation process for all subjects will include a comprehensive functional assessment, setting short-term and long-term individualized goals for each subject, prescribing and implementing a primary outpatient rehabilitation plan involving various rehabilitative interventions. Once the plan is implemented, the physical medicine and rehabilitation (PMR) physician will thoroughly assess the rehabilitation results. An observation period will follow, during which learned self-help techniques will be integrated into daily life. After six months, all subjects will be reassessed by a PMR physician.
Process:
After inclusion, all participants will be thoroughly assessed by a qualified PMR physician specializing in pelvic floor dysfunction rehabilitation. Following all functional assessments, an individualized primary outpatient rehabilitation plan will be agreed upon with the patient, comprising 20 rehabilitative interventions. Depending on the group to which the subject is randomized, the individualized rehabilitation interventions will either consist of classical interventions (such as physiotherapy, occupational therapy, electrical stimulation, etc.) for the control group, or classical interventions combined with modern physical agents for the interventional group.
During the rehabilitation period, the rehabilitation team will monitor subjects in both groups for any side effects from the rehabilitation interventions. Subjects will also have the option to inform and consult a PMR physician as often as needed in case of side effects or intolerance to prescribed interventions.
The PMR physician will conduct thorough functional assessments again after rehabilitation and after six months.
Methods to assess functioning and pelvic floor dysfunctions:
Before rehabilitation:
Detailed questioning regarding the history of pelvic floor dysfunction, other treatments received, general health, and relevant psychosocial factors will precede setting an individualized rehabilitation plan for pelvic floor dysfunctions. The four-item patient health questionnaire for anxiety and depression ( PHQ-4 ) will be used when indicated. Subjects may be asked to fill out a 3-day bladder diary, a diary on bowel incontinence events, a male patients' diary on erection/ejaculation quality and satisfaction with sexual activity, or a pain questionnaire covering pain diagrams and intensity assessments, questions on pain quality, duration, and exacerbation/or alleviation factors, and changes over time.
A trained PMR physician will conduct a thorough clinical examination (including posture, perineum, and digital external and internal pelvic floor muscle assessment) and, when possible, functional testing of slow and quick muscle fibers endurance.
Functional assessment of the abdominal wall (for diastasis, abdominal muscle activity during a curl-up task, straight leg raise task) and pelvic floor muscle morphological and functional evaluation will be performed using two and three-dimensional (2D/3D) ultrasound (transabdominal and transperineal).
After rehabilitation:
To assess subjective experiences and attitudes towards received outpatient rehabilitation, all subjects will complete a self-reported questionnaire about symptom improvement based on global improvement rating scales. The questionnaire will also contain open-ended questions about patient expectations, experiences with learned self-help techniques, attitudes, and suggestions for the rehabilitation team regarding pelvic floor dysfunction rehabilitation. Subjects will rate the perceived helpfulness of each received rehabilitative intervention on a numeric 0-10 scale (where 0 is 'not helpful at all' and 10 is 'maximally helpful').
A thorough clinical examination (including perineum, digital external and internal pelvic floor muscle assessment) and, when possible, functional testing of slow and quick muscle fibers endurance will be conducted by a trained PMR physician.
Functional assessment of the abdominal wall (for diastasis), abdominal muscles, and pelvic floor muscle morphological and functional evaluation will be performed using 2D/3D ultrasound (transabdominal and transperineal).
When indicated (depending on symptoms and dysfunctions), subjects may be asked to fill out a 3-day bladder diary, a pain questionnaire, or diaries on bowel incontinence events and male sexual function.
The PHQ-4 will be used.
After six months:
detailed questionnaire on changes in pelvic floor dysfunction symptoms post-rehabilitation, other treatments received, general health, and other psychosocial factors will be conducted by a PMR physician to determine if further rehabilitation interventions are necessary. When indicated, subjects may be asked to fill out a 3-day bladder diary, a pain questionnaire, or other condition-specific diaries.
The PHQ-4 will be used for all subjects. A thorough clinical examination (including perineum, digital external and internal pelvic floor muscle assessment) and, when possible, functional testing of slow and quick muscle fibers endurance will be conducted by a trained PMR physician.
Functional assessment of the abdominal wall (for diastasis), abdominal muscles, and pelvic floor muscle
Interventions
- Other modern agents rehab
rehabilitation interventions containing modern physical agents together with classical interventions - Other classical rehab
classical rehabilitation interventions
Primary outcome measures
- Overall change in bothering pelvic floor symptoms according to Global Rating of Change (GRC) scales [Time frame: 3 months]
Secondary outcome measures (12)
- Overall change in urinary dysfunction symptoms [Time frame: 3 months and 6 months]
- Overall change in fecal incontinence [Time frame: 3 months and 6 months]
- Overall change in pelvic pain [Time frame: 3 months and 6 months]
- Overall change in male sexual function [Time frame: 3 months and 6 months]
- Change in pelvic floor muscle contraction: ability to contract and relax pelvic floor muscles [Time frame: 3 months and 6 months]
- Change in pelvic floor painfulness from palpation [Time frame: 3 months and 6 months]
- Change in pelvic floor muscle endurance [Time frame: 3 months and 6 months]
- Change in pelvic floor muscle strenght [Time frame: 3 months and 6 months]
- Change in diastasis recti [Time frame: 3 months and 6 months]
- Change in vestibular painfulness [Time frame: 3 months and 6 months]
- Number of participants with treatment-related adverse events as assessed by CTCAE v5.0 [Time frame: Throughout rehabilitation and at 3 months and 6 months]
- Individual subjects perceptions regarding the helpfulness of the rehabilitation interventions in reducing pelvic floor dysfunction symptoms and enhancing overall functioning [Time frame: 3 months]
Eligibility criteria
Inclusion criteria
- Patients older than 18 years old.
- One or more signs characteristic of pelvic floor dysfunctions are identified: elimination function disorders, pelvic organ prolapse, scar(s) (and lack of tissue mobility) in the perineum, pelvic floor muscle tone/strength disorders (hypoactivity/hyperactivity), neuromuscular control disorders, sexual dysfunctions, pain in the pelvis, perineum.
- Not a single exclusion criterion has been established.
- Subjects capable of signing informed consent.
Exclusion criteria
- Oncological diseases or being actively investigated for oncological diseases.
- Any contraindications to methods of functional state examination or physical agents in the pelvic area that will be used in the study
- Individuals who refuse a detailed clinical examination of the perineum and pelvic floor muscles, functional testing, and/or functional ultrasound examination.
- Patients with urinary tract, prostate, genital, and other infections.
- Patients with inflammatory bowel diseases (ulcerative colitis, Crohn's disease, etc.).
- Persons for whom other health care professionals have already planned treatment of pelvic dysfunctions or other diseases during the expected participation period in the study that may interfere with participation in the study and/or significantly change the health status of the patient's pelvic floor.
- Pregnant or planning to become pregnant during the expected period of rehabilitation interventions.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Open label
- Primary purpose
- Treatment
Study locations
Lithuania · 1 center
- Hospital of Lithuanian University of Health Sciences Kaunas Clinics — Kaunas
Identifiers
NCT: NCT06800222 · P-02 V-3