Skip to content

Diaphragm Function and Urinary Incontinence in Stroke

Investigation of the Relationship Between Diaphragm Muscle Function and Urinary Incontinence in Stroke Patients

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07048210
Enrollment
50
Registered
2025-07-02
Start date
2025-06-30
Completion date
2025-09-29
Last updated
2025-07-02

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

Conditions

Stroke

Keywords

Diaphragm, Urinary Incontinence, Stroke, Respiratory Function

Brief summary

Stroke affects respiratory functions by causing structural and strength impairments in both inspiratory and expiratory respiratory muscles. Weakening of the diaphragm leads to a decrease in maximal inspiratory pressure (MIP) and maximal expiratory pressure (MEP), which may result in respiratory insufficiency, postural instability, and urinary incontinence (UI). Additionally, post-stroke reduction in diaphragmatic mobility and decreased activity of the diaphragm and abdominal muscles on the paretic side may disrupt the piston mechanism between the diaphragm and pelvic floor muscles. These mechanical changes may trigger the development of urinary incontinence. This study aims to investigate the relationship between diaphragm muscle strength and endurance and urinary incontinence in 50 stroke patients. In addition, diaphragmatic function and posture-related respiratory changes will be evaluated using functional tests based on the Dynamic Neuromuscular Stabilization (DNS) approach. The relationship between respiratory muscle strength (MIP, MEP) and endurance and the scores of the Urogenital Distress Inventory (UDI-6) and the Incontinence Impact Questionnaire (IIQ-7) will be analyzed. Furthermore, individuals with and without urinary incontinence symptoms will be evaluated in terms of diaphragmatic function and contribution to respiration.

Interventions

None listed

Sponsors

Istinye University
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
40 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Aged between 40 and 75 years, * Diagnosed with hemorrhagic or ischemic stroke confirmed by computed tomography (CT) or magnetic resonance imaging (MRI) conducted by a specialist physician, * Presence of urinary incontinence, * No other orthopedic, rheumatologic, or neurological diagnoses apart from stroke, * Ability to understand the investigator's instructions and a score of ≥24 on the Mini-Mental State Examination (MMSE), * Voluntary participation in the study, * Ability to speak and understand Turkish.

Exclusion criteria

* Presence of serious diseases affecting vital organs such as the heart, lungs, liver, or kidneys, * Presence of a genitourinary infection, * Pelvic organ prolapse at stage 3 or higher, * Uncontrolled cardiopulmonary or unstable chronic diseases, * Presence of one or more neurological disorders that may cause balance impairments, * Severe cognitive, speech, or visual impairments, * History of urogynecological surgery within the past 6 months, * History of abdominal surgery within the past 6 months.

Design outcomes

Primary

MeasureTime frameDescription
Diaphragm Muscle FunctionBaseline (single assessment)Diaphragm muscle function will be assessed using the Dynamic Neuromuscular Stabilization (DNS) approach. The evaluation consists of three components: (1) the diaphragm's contribution to respiration, (2) its role in postural stabilization, and (3) active respiration during postural stabilization. Each component will be rated separately using a 4-point scale: none (3), mild (2), moderate (1), and severe (0). Higher total scores reflect greater impairment in diaphragm-related respiratory function.
Urogenital Distress Inventory (UDI-6)Baseline (single assessment)The Urogenital Distress Inventory (UDI-6) consists of 6 items and is rated on a four-point Likert scale. The total score ranges from 0 to 18, with higher scores indicating greater symptom distress and a more impaired quality of life.
Incontinence Impact Questionnaire (IIQ-7)Baseline (single assessment)The Incontinence Impact Questionnaire (IIQ-7) consists of 7 items and is rated on a four-point Likert scale. The total score ranges from 0 to 21, with lower scores indicating less impact on quality of life.

Secondary

MeasureTime frameDescription
Respiratory Muscle StrengthBaseline (single assessment)Respiratory muscle strength will be assessed using a portable device capable of measuring maximal inspiratory (MIP) and expiratory (MEP) mouth pressures electronically (MicroRPM, Micro Medical, Kent, UK). Measurements will be conducted with the participant in a seated position, wearing a nose clip to prevent air leakage. For MIP, the participant will perform a maximal exhalation followed by a maximal inhalation against an occluded airway for at least 1.5 seconds. For MEP, a maximal inhalation will be followed by a maximal exhalation under the same conditions. Each measurement will be repeated three times with less than 10% variability, and the highest value will be used for analysis.
Respiratory Muscle EnduranceBaseline (single assessment)Respiratory muscle endurance will be assessed using a threshold loading test with the PowerBreathe device (HaB International Ltd., Southam, UK). The test will begin at 20% of the participant's maximal inspiratory pressure (MIP) and will be increased in two-minute intervals to 40%, 60%, 80%, and finally 100% of MIP. During the test, the device will be placed in the participant's mouth and a nose clip will be used to prevent nasal breathing. Participants will be instructed to breathe through the mouth for 10 minutes. Oxygen saturation and perceived dyspnea will be measured before the test, at the end of each two-minute stage, and after the test. Test results will be calculated by multiplying the total test duration by the corresponding pressure level at each stage.

Contacts

Primary ContactÖzge Çakmak, MSc
ozgeckmakk@gmail.com+905359463069
Backup ContactYunus Emre Tütüneken
yunus.tutuneken@istinye.edu.tr+905435912455

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 19, 2026