Ignite Creation Date:
2024-05-06 @ 7:53 PM
Last Modification Date:
2024-10-26 @ 3:16 PM
Study NCT ID:
NCT06172439
Status:
COMPLETED
Last Update Posted:
2024-06-26
First Post:
2023-12-07
Brief Title:
Effect of Acupressure on Postoperative Pain With Gynecologıcal Surgery
Sponsor:
Saglik Bilimleri Universitesi
Organization:
Saglik Bilimleri Universitesi
Study Overview
Official Title:
The Effect Of Acupressure Applıcatıon On Postoperative Pain Level İn Women With Abdominal Gynecologıcal Surgery Randomized Controlled Study
Status:
COMPLETED
Status Verified Date:
2024-06
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:
In this study the effect of acupressure on postoperative pain level in women with abdominal gynecologıcal surgery will be studied and it will be conducted as a randomized controlled intervention study to examine the relationships with each otherThe sample group will consist of 102 women 51 in the intervention group and 51 in the control groupWithin the scope of the study the data will be collected using the Personal Information Form and Short-Form McGill Pain Questionnaire SF-MPQ created by the researcher Data will be analyzed using SPSS-26 package
Detailed Description:
In this study the effect of acupressure on postoperative pain level in women with abdominal gynecologıcal surgery will be studied and it will be conducted as a randomized controlled intervention study to examine the relationships with each otherThe sample group will consist of 102 women 51 in the intervention group and 51 in the control groupWithin the scope of the study the data will be collected using the Personal Information Form and Short-Form McGill Pain QuestionnaireSF-MPQ created by the researcher Data will be obtained by the researcher by faceto-face interviews with women In addition women in the intervention group will receive acupressure once on postoperative days 0 and 1 Acupressure points related to gynecological surgery large intestine LI4 stomach ST36 and spleen SP6 will be applied for a total of 12 minutes with 2 minutes of pressure on each point Women in the control group will continue their routine care Data will be evaluated with SPSS-26 package
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