- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT07710508
Difference in Incontinence Prevalence Between High Impact Athletes, Low Impact Athletes and Sedentary Subjects.
Difference in Incontinence Prevalence Between High Impact Athletes, Low Impact Athletes and Sedentary Subjects. A Functional Analysis.
This observational cross-sectional study aims to investigate the association between participation in high-impact sports, physical activity level, and urinary incontinence in young adults. The study will compare six groups based on sex and physical activity level: male and female high-impact sports participants, physically active males and females who do not participate in high-impact sports, and sedentary males and females.
Participants aged 18-35 years will undergo a single assessment including sociodemographic and medical information, physical activity assessment, urinary incontinence questionnaires, sport-related characteristics, psychosocial questions regarding the influence of social taboos on questionnaire responses, lower-limb muscle strength testing using a load cell, and vertical jump performance assessment.
The study aims to describe the prevalence, severity, type, and impact of urinary incontinence across different activity levels and sexes, and to explore potential associations with lower-limb strength, jump performance, and sport-related characteristics.
Studienübersicht
Status
Bedingungen
Intervention / Behandlung
Detaillierte Beschreibung
Urinary incontinence is a common condition that may affect both women and men and has been associated with physical activity and participation in high-impact sports. Although regular exercise provides substantial health benefits, repetitive increases in intra-abdominal pressure during high-impact activities may contribute to pelvic floor dysfunction in susceptible individuals. Most previous studies have focused on female athletes from specific sports, while evidence including both sexes and different physical activity levels remains limited.
This observational cross-sectional study will compare urinary incontinence characteristics among six population groups defined according to sex and physical activity level: male and female participants in high-impact sports, physically active males and females who do not participate in high-impact sports, and sedentary males and females.
Participants will attend a single face-to-face assessment session after providing written informed consent. During the visit, sociodemographic and clinical information, physical activity characteristics, sport-related variables, urinary incontinence questionnaires, and psychosocial questions related to social taboos and response honesty will be collected. Lower-limb muscle strength will be assessed using a load cell system, and jump performance will be evaluated using the My Jump 2 application.
The primary objective is to compare the prevalence, severity, type, and impact of urinary incontinence across the different study groups. Secondary analyses will explore the relationship between urinary incontinence and physical activity level, lower-limb muscle strength, jump performance, sport-related characteristics, and selected demographic and clinical variables.
Participants will be recruited through social media, institutional dissemination, and sports clubs using voluntary convenience and snowball sampling. All assessments will be performed by trained researchers following standardized procedures.
Studientyp
Einschreibung (Geschätzt)
Kontakte und Standorte
Studienorte
-
-
Valencia
-
Valencia, Valencia, Spanien, 46010
- Gascó Oliag, 5
-
-
Teilnahmekriterien
Zulassungskriterien
Studienberechtigtes Alter
- Erwachsene
Akzeptiert gesunde Freiwillige
Probenahmeverfahren
Studienpopulation
Beschreibung
Inclusion Criteria:
- Adults aged 18 to 35 years.
- Male or female participants.
- Able to understand and provide written informed consent.
- Belong to one of the following groups:
Regular participation in high-impact sports (≥2 training sessions per week for at least the previous 2 years).
Physically active individuals meeting the World Health Organization recommendations (≥150 minutes/week of moderate-intensity activity, ≥75 minutes/week of vigorous-intensity activity, or an equivalent combination), without regular participation in high-impact sports.
Sedentary individuals who do not meet the World Health Organization physical activity recommendations.
Exclusion Criteria:
- Pregnancy or childbirth within the previous 12 months.
- Current or recent urinary tract infection.
- History of urogynecological disease or pelvic/urogynecological surgery.
- Body mass index (BMI) >35 kg/m².
- Inability to understand or complete the study procedures or questionnaires in Spanish or English.
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
Kohorten und Interventionen
Gruppe / Kohorte |
Intervention / Behandlung |
|---|---|
|
Male High-Impact Sports Participants
Males aged 18-35 years who regularly participate in high-impact sports (at least twice per week for the previous two years).
|
No intervention
|
|
Female High-Impact Sports Participants
Females aged 18-35 years who regularly participate in high-impact sports (at least twice per week for the previous two years).
|
No intervention
|
|
Physically Active Males
Males aged 18-35 years who meet the World Health Organization physical activity recommendations but do not participate in high-impact sports.
|
No intervention
|
|
Physically Active Females
Females aged 18-35 years who meet the World Health Organization physical activity recommendations but do not participate in high-impact sports.
|
No intervention
|
|
Sedentary Males
Males aged 18-35 years who do not meet the World Health Organization physical activity recommendations.
|
No intervention
|
|
Sedentary Females
Females aged 18-35 years who do not meet the World Health Organization physical activity recommendations.
|
No intervention
|
Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Urinary incontinence severity
Zeitfenster: Baseline (single study visit)
|
Urinary incontinence severity assessed using the International Consultation on Incontinence Questionnaire-Urinary Incontinence Short Form (ICIQ-UI SF).
Higher scores indicate greater symptom severity and impact on quality of life.
The total score ranges from 0 to 21, with higher scores indicating more severe urinary incontinence symptoms and greater impact on quality of life.
|
Baseline (single study visit)
|
Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Urinary incontinence-related quality of life
Zeitfenster: Baseline (single study visit)
|
Quality of life associated with urinary incontinence assessed using the Incontinence Quality of Life Questionnaire (I-QOL).
The total score ranges from 0 to 100, with higher scores indicating better urinary incontinence-related quality of life.
|
Baseline (single study visit)
|
|
Lower-limb muscle strength
Zeitfenster: Baseline (single study visit)
|
Maximum voluntary force and mean voluntary force of hip adduction, abduction, flexion, extension, internal rotation, and external rotation measured using a load cell and ChronoJump software.
|
Baseline (single study visit)
|
|
Vertical jump performance
Zeitfenster: Baseline (single study visit)
|
Vertical jump performance assessed using the My Jump 2 application.
|
Baseline (single study visit)
|
|
Physical activity level
Zeitfenster: Baseline (single study visit)
|
Physical activity level assessed using the International Physical Activity Questionnaire (IPAQ).
Physical activity is expressed as metabolic equivalent (MET)-minutes per week and classified into low, moderate, or high physical activity levels, according to the IPAQ scoring protocol.
Higher MET-minutes per week indicate greater levels of physical activity.
|
Baseline (single study visit)
|
Mitarbeiter und Ermittler
Sponsor
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn (Tatsächlich)
Primärer Abschluss (Geschätzt)
Studienabschluss (Geschätzt)
Studienanmeldedaten
Zuerst eingereicht
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst gepostet (Tatsächlich)
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Zuletzt verifiziert
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Schlüsselwörter
Zusätzliche relevante MeSH-Bedingungen
- Urogenitale Erkrankungen
- Männliche Urogenitalerkrankungen
- Urologische Erkrankungen
- Weibliche Urogenitalerkrankungen
- Weibliche Urogenitalerkrankungen und Schwangerschaftskomplikationen
- Störungen beim Wasserlassen
- Symptome der unteren Harnwege
- Urologische Manifestationen
- Pathologische Zustände, Anzeichen und Symptome
- Verhalten
- Anzeichen und Symptome
- Harninkontinenz
- Harninkontinenz, Stress
- Motorik
Andere Studien-ID-Nummern
- Sports_UI
Plan für individuelle Teilnehmerdaten (IPD)
Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?
Arzneimittel- und Geräteinformationen, Studienunterlagen
Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt
Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt
Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .
Klinische Studien zur Harninkontinenz, Stress
-
University of Thi-QarAbgeschlossenPsychologischer Stress | Akademischer StressIrak
-
Canterbury Christ Church UniversitySussex Partnership NHS Foundation TrustAnmeldung auf EinladungBeruflicher Stress oder Stress am ArbeitsplatzVereinigtes Königreich
-
Universita di VeronaUniversity of Roma La SapienzaRekrutierungStress, emotional | Stress, PsychischItalien
-
Massachusetts General HospitalAbgeschlossenBetonen | Emotionaler Stress | Psychologischer Stress | Sozialer Stress | LebensstressVereinigte Staaten
-
Inspiration at WorkNorthwestern UniversityAbgeschlossenStress, emotional | Job-StressVereinigte Staaten
-
Maharishi International UniversityCenter for Wellness and Achievement in EducationAbgeschlossenJob-Stress | Wahrgenommener Stress
-
Amsterdam UMC, location VUmcRigshospitalet, Denmark; Universitätsklinikum Hamburg-EppendorfNoch keine RekrutierungBetonen | Stress und Burnout | Stress BiomarkerDeutschland, Dänemark
-
Kamuran CeritNoch keine RekrutierungAchtsamkeitsbasiertes Programm für Stress, Zufriedenheit und Leistung von Pflegekräften (MIND-NURSE)Job-Stress | Arbeitszufriedenheit | Arbeitsleistung
-
Egas Moniz - Cooperativa de Ensino Superior, CRLAnmeldung auf EinladungAusbrennen | Burnout Syndrom | Beruflicher Stress oder Stress am ArbeitsplatzPortugal
-
Holly RisdonBPAi; American Institute of StressNoch keine Rekrutierung
Klinische Studien zur No Intervention: Observational Cohort
-
RTI InternationalNo Means No WorldwideAbgeschlossenSexuelle Gewalt | Geschlechtsspezifische GewaltSüdafrika
-
University of Illinois at ChicagoUniversity of Chicago; The Broad FoundationAbgeschlossenColitis ulcerosaVereinigte Staaten
-
King's College LondonMedical University of Graz; Radboud University Medical Center; Novo Nordisk A/S; Juvenile Diabetes Research Foundation und andere MitarbeiterAbgeschlossenDiabetes mellitus, Typ 2 | Hypoglykämie | Diabetes mellitus, Typ 1 | Hypoglykämie-WahrnehmungsstörungVereinigtes Königreich
-
Seattle Institute for Biomedical and Clinical ResearchNational Institute on Alcohol Abuse and Alcoholism (NIAAA); University of Washington und andere MitarbeiterAbgeschlossenAlkoholismus | Belastungsstörungen, posttraumatischVereinigte Staaten