Ignite Creation Date:
2024-05-06 @ 8:21 PM
Last Modification Date:
2025-12-17 @ 4:32 AM
Study NCT ID:
NCT06342154
Status:
None
Last Update Posted:
2024-04-02 00:00:00
First Post:
2024-03-22 00:00:00
Brief Title:
Does Endorphin Massage Reduce the Anxiety of Pregnant Women?
Sponsor:
Celal Bayar University
Organization:
Celal Bayar University
Study Overview
Official Title:
Does Endorphin Massage Applied Before Cesarean Section Reduce the Anxiety of Pregnant Women?
Status:
None
Status Verified Date:
2024-03
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The sample size of the research was calculated using G\*Power 3.1.9.4 software as a minimum of 34 with 95% power, 0.01 alpha, and 0.9 effect size. The sample size was planned as experimental (n=34) and control (n=34) groups. To ensure the equality of the samples in both groups, a simple randomization method was used, where pregnant women with odd hospital protocol numbers will be included in the experimental group and those with even numbers will be included in the control group. Pregnant women who are admitted for pre-cesarean section care will be informed about the study, and their voluntary consent will be obtained both in written and verbal form. Pre-tests will be administered to both the experimental and control groups at 08:00, and blood samples will be taken to measure cortisol levels. Subsequently, an intervention will be applied to those in the experimental group, while those in the control group will receive routine nursing care. At 09:00, post-tests will be administered to both the experimental and control groups, and blood samples will be taken again to measure cortisol levels. The pre-test and post-test results, as well as the mean cortisol levels, will be compared between the experimental and control groups.
Detailed Description:
The sample size of the research was calculated using GPower 3194 software as a minimum of 34 with 95 power 001 alpha and 09 effect size The sample size was planned as experimental n34 and control n34 groups To ensure the equality of the samples in both groups a simple randomization method was used where pregnant women with odd hospital protocol numbers will be included in the experimental group and those with even numbers will be included in the control group Pregnant women who are admitted for pre-cesarean section care will be informed about the study and their voluntary consent will be obtained both in written and verbal form Pre-tests will be administered to both the experimental and control groups at 0800 and blood samples will be taken to measure cortisol levels Subsequently an intervention will be applied to those in the experimental group while those in the control group will receive routine nursing care At 0900 post-tests will be administered to both the experimental and control groups and blood samples will be taken again to measure cortisol levels The pre-test and post-test results as well as the mean cortisol levels will be compared between the experimental and control groups
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None