Pain Clinical Trial
Official title:
The Effect of Using a Stress Ball During Vaginal Examination on Anxiety and Pain Levels
NCT number | NCT06263166 |
Other study ID # | 5535 |
Secondary ID | |
Status | Not yet recruiting |
Phase | N/A |
First received | |
Last updated | |
Start date | March 2024 |
Est. completion date | December 2024 |
Verified date | February 2024 |
Source | Ondokuz Mayis University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Women who will undergo vaginal examinations randomly assigned to intervention (n = 44) and control (n = 44) groups at a public hospital in Turkey will participate in the study. Stress ball application before vaginal examination will be explained to women in the intervention group. These women will be asked to tighten and loosen the stress ball given to them during the vaginal examination and continue this process until the examination is completed. Data regarding pain and anxiety outcomes will be collected before and after the examination. The main questions it aims to answer are: - question 1: What is the effect of stress ball application on women's anxiety level during vaginal examination? - question 2: What is the effect of stress ball application on women's pain level during vaginal examination?
Status | Not yet recruiting |
Enrollment | 88 |
Est. completion date | December 2024 |
Est. primary completion date | August 2024 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | 18 Years to 65 Years |
Eligibility | Inclusion Criteria: - Volunteer to participate in the research, - Those between the ages of 18-65, - Applying to the polyclinic for vaginal examination, - It is planned to recruit women who can read and write Turkish. Exclusion Criteria: - Pregnant, - Having a diagnosed psychiatric problem such as depression, anxiety disorder, panic attack, bipolar affective disorder or schizophrenia - It is planned to exclude women with visual, hearing, speech, physical, or mental disabilities. |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Ondokuz Mayis University |
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* Note: There are 17 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Anxiety change | As assessed by the State-Trait Anxiety Inventory (STAI) STAI consists of two scales, a total of 40 self-reported items. The State Anxiety Scale only used in this study, consists of 20 straight and inverse scored terms, and is scored between 20 and 80 in a likert type scoring between 1 and 4. High scores indicate high anxiety levels. | Immediately after the intervention | |
Primary | Pain level | Visual Analog Scale (VAS) will be used to determine the severity of pain experienced by women in the intervention and control groups during vaginal examination. VAS converts values that cannot be measured numerically into numerical values. This scale is widely used for pain assessment. The pain level varies between 0 and 10, and an increase in the marked numerical value indicates an increase in the pain level. In the VAS evaluation, 0 = no pain, 1-4 = mild pain, 5-6 = moderate pain, and 7-10 = severe pain. | Immediately after the intervention |
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