NCT07330739

Brief Summary

All women included in the study will be administered the Causes of Kinesiophobia Scale (KCS), the International Physical Activity Questionnaire (Short), the International Incontinence Consultation Questionnaire-Short Form (ICIQ-SF), and the Pittsburgh Sleep Quality Questionnaire (PSQI). Subsequent analysis will determine the causes of kinesiophobia in women with urinary incontinence.

Trial Health

55
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
112

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Nov 2025

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
active not recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

November 20, 2025

Completed
1 month until next milestone

First Submitted

Initial submission to the registry

December 21, 2025

Completed
19 days until next milestone

First Posted

Study publicly available on registry

January 9, 2026

Completed
11 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 20, 2026

Completed
21 days until next milestone

Study Completion

Last participant's last visit for all outcomes

February 10, 2026

Completed
Last Updated

January 9, 2026

Status Verified

January 1, 2026

Enrollment Period

2 months

First QC Date

December 21, 2025

Last Update Submit

January 5, 2026

Conditions

Kinesiophobia

Outcome Measures

Primary Outcomes (1)

  • Kinesiophobia

    Kinesiophobia, or fear of movement, in patients will be assessed using the Causes of Kinesiophobia Scale. This scale consists of 20 questions and evaluates the fear of movement in two subcategories: biological and psychological causes.

    day 1

Study Arms (2)

Stress Urinary Incontinence

Other: Survey

Control

Other: Survey

Interventions

SurveyOTHER

survey

ControlStress Urinary Incontinence

Eligibility Criteria

Age18 Years - 65 Years
Sexfemale(Gender-based eligibility)
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

women with stress urinary incontinence

You may qualify if:

  • Being between 18-65 years old
  • Having stress urinary incontinence
  • Voluntary participation in the study

You may not qualify if:

  • Unwillingness to continue working
  • Presence of neurological or orthopedic disease
  • Learning disability or other cognitive impairments.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Kirşehir Ahi Evran University Physical Therapy and Rehabilitation Hospital

Kırşehir, Centre, 40000, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Kinesiophobia

Interventions

Surveys and Questionnaires

Condition Hierarchy (Ancestors)

Phobic DisordersAnxiety DisordersMental Disorders

Intervention Hierarchy (Ancestors)

Data CollectionEpidemiologic MethodsInvestigative TechniquesHealth Care Evaluation MechanismsQuality of Health CareHealth Care Quality, Access, and EvaluationPublic HealthEnvironment and Public Health

Study Officials

  • ESRA bayramoğlu demirdöğen

    Kirsehir Ahi Evran Universitesi

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
CASE CONTROL
Time Perspective
PROSPECTIVE
Target Duration
3 Months
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
LECTURER DOCTOR

Study Record Dates

First Submitted

December 21, 2025

First Posted

January 9, 2026

Study Start

November 20, 2025

Primary Completion

January 20, 2026

Study Completion

February 10, 2026

Last Updated

January 9, 2026

Record last verified: 2026-01

Data Sharing

IPD Sharing
Will not share

Locations

TU(1)