Status:
UNKNOWN
Effect of Stress Ball Use on Anxiety Level During Endometrial Biopsy Procedure
Lead Sponsor:
Zonguldak Bulent Ecevit University
Conditions:
Biopsy Wound
Endometrial Hyperplasia
Eligibility:
FEMALE
18+ years
Phase:
NA
Brief Summary
The aim of this study is to determine the effect of stress ball application on the anxiety level during the endometrial biopsy procedure. This research is planned as a randomised controlled study. Pl...
Detailed Description
Endometrial biopsy is a simple, inexpensive and effective method to rule out endometrial cancer. Endometrial biopsy is the gold standard method in the diagnosis of endometrial pathologies and is wide...
Eligibility Criteria
Inclusion
- EXPERIMENT GROUP
- Willingness to participate in the research
- 18 years of age or older
- Reading and writing Turkish
- No active mental illness preventing data collection
- No impediment to squeezing the ball
- No emergency and risky situation that will prevent data collection during the process CONTROL GROUP
- Willingness to participate in the research
- 18 years of age or older
- Reading and writing Turkish
- No active mental illness preventing data collection
- No emergency and risky situation that will prevent data collection during the process
Exclusion
- INTERVENTION GROUP
- Not willing to participate in the research
- Under 18 years of age
- Not knowing how to read and write Turkish
- Having an active mental illness that prevents data collection
- Having an obstacle to squeezing the ball
- The development of an urgent and risky situation that will prevent data collection during the process CONTROL GROUP
- Not willing to participate in the research
- Under 18 years of age
- Not knowing how to read and write Turkish
- Having an active mental illness that prevents data collection
- The development of an urgent and risky situation that will prevent data collection during the process
Key Trial Info
Start Date :
February 1 2024
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
March 1 2024
Estimated Enrollment :
70 Patients enrolled
Trial Details
Trial ID
NCT06171581
Start Date
February 1 2024
End Date
March 1 2024
Last Update
January 9 2024
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