KinesiophobiaNCT07330739
Kinesiophobia in Women With Stress Urinary Incontinence
An observational study of Kinesiophobia, run by Esra BAYRAMOĞLU DEMİRDÖĞEN at 1 site in Turkey (Türkiye).
Trial 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). Read more about this study
- Who is it for?
- Ages 18 to 65 years, women onlyHealthy volunteers can take part
- Conditions the study is for
- Kinesiophobia
- What is being tested?
- Survey
- How many people
- 115 participants
- Where
- 1 siteTurkey (Türkiye)
- Study dates
- 20 Nov 2025to 10 Feb 2026
- How long will I take part?
- 3 Months
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 65 years
- Women only
- Healthy volunteers accepted
- Adult, Older adult
Study population: women with stress urinary incontinence
Who may be able to join
- Being between 18-65 years old
- Having stress urinary incontinence
- Voluntary participation in the study
Who cannot join
- Unwillingness to continue working
- Presence of neurological or orthopedic disease
- Learning disability or other cognitive impairments.
Trial locations and contacts
1 site in 1 country.
Turkey (Türkiye)1 site
Kirşehir Ahi Evran University Physical Therapy and Rehabilitation Hospital
Kırşehir, Centre, 40000
About this study
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.
Read the detailed description
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. The results will then be compared with those of healthy women.
- Conditions
- Kinesiophobia
- Being tested
- Survey
- Medical subject headings
- Kinesiophobia
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
SurveyOther
survey
| Study group | Role | What they receive |
|---|---|---|
| Stress Urinary Incontinence | intervention Receives: Other: Survey | |
| Control | Healthy Receives: Other: Survey |
What is being measured
The primary outcome is the main question the study is designed to answer.
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.
Measured: day 1
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted9 Jan 2026
- Study start20 Nov 2025
- Primary completion20 Jan 2026
- Study completion10 Feb 2026
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for KinesiophobiaStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Case-control
- Time perspective
- Prospective
- Enrolment
- 115 participants (actual)
- Target duration
- 3 Months
Sponsor and investigators
- Lead sponsor
- Esra BAYRAMOĞLU DEMİRDÖĞEN
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor-investigator, Esra BAYRAMOĞLU DEMİRDÖĞEN, Ahi Evran University Education and Research Hospital
- Investigators
- ESRA bayramoğlu demirdöğen, Principal investigator, Kirsehir Ahi Evran Universitesi
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07330739
- Sponsor's protocol ID
- KAEU-EBAYRAMOGLUD-005
- Status last verified
- Aug 2026
- First submitted
- 21 Dec 2025
- Last updated
- 6 Aug 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 6 Aug 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Kinesiophobia in Women With Stress Urinary Incontinence
- ClinicalTrials.gov ID
- NCT07330739
- Acronym / sponsor ID
- KAEU-EBAYRAMOGLUD-005
- Conditions
- Kinesiophobia
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 115 participants (actual)
- Lead sponsor
- Esra BAYRAMOĞLU DEMİRDÖĞENUniversity, hospital or other
- Study start
- 20 Nov 2025 (actual)
- Primary completion
- 20 Jan 2026 (actual)
- Study completion
- 10 Feb 2026 (actual)
- First posted
- 9 Jan 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
Detailed description
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. The results will then be compared with those of healthy women.
Study design
- Observational model
- Case-control
- Time perspective
- Prospective
- Target follow-up
- 3 Months
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Stress Urinary Incontinence | – | Other: Surveyintervention |
| Control | – | Other: SurveyHealthy |
Who may qualify
- Ages
- 18 to 65 years
- Sex
- Female only
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
- Study population
- women with stress urinary incontinence
Key inclusion criteria (3 listed)
- Being between 18-65 years old
- Having stress urinary incontinence
- Voluntary participation in the study
Key exclusion criteria (3 listed)
- Unwillingness to continue working
- Presence of neurological or orthopedic disease
- Learning disability or other cognitive impairments.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Surveysurvey | Other | Control, Stress Urinary Incontinence |
Primary outcome
Kinesiophobia
Time frame: day 1
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.
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 6 Aug 2026.
- Individual participant dataSharing planned: No
Related trials for Kinesiophobia
Recruiting
Effects of Virtual Reality Environments on Walking in Adults With and Without Knee Osteoarthritis
Knee Osteoarthritis
Recruiting
Effects of Pelvic Floor Muscle Training and a Modified Lumbopelvic Belt on Pain, Kinesiophobia, and Functional Status in Pregnant Women With Symphysis Pubis Pain
Symphysis Pubis Dysfunction, Pregnancy
Not yet recruiting
Multicomponent Exercise and Pain Science Education for Fall Prevention in Older Adults With Chronic Musculoskeletal Pain (MovePainFall)
Chronic Pain, Musculoskeletal Pain
Not yet recruiting
Effects of Transcranial Direct Current Stimulation and Manual Therapy on Musculoskeletal Pain in Adolescent Dancers
Musculoskeletal Pain, Chronic Pain
Active, not recruitingObservational study
The Impact of Osteosarcopenia on Falls, Kinesiophobia, and Quality of Life in Postmenopausal Women
Osteosarcopenia, Sarcopenia
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
ESRA bayramoğlu demirdöğen principal investigator
Kirsehir Ahi Evran Universitesi
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Kinesiophobia, run by Esra BAYRAMOĞLU DEMİRDÖĞEN at 1 site in Turkey (Türkiye).
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 3 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 6 Aug 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Kinesiophobia (time frame: day 1). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 6 Aug 2026.