Ignite Creation Date:
2024-05-19 @ 5:34 PM
Last Modification Date:
2024-10-26 @ 3:29 PM
Study NCT ID:
NCT06415162
Status:
RECRUITING
Last Update Posted:
2024-05-16
First Post:
2024-05-10
Brief Title:
Evaluation of the Effects of Using Cooling Pillowcases on the Symptoms of Hot Flushes Sleep and Life Quality
Sponsor:
Saglik Bilimleri Universitesi
Organization:
Saglik Bilimleri Universitesi
Study Overview
Official Title:
Evaluation of the Effects of Education on Side Effects Management and the Use of Cooling Pillowcases on Hot Flash Complaints Sleep and Quality of Life in Women With Breast Cancer Receiving Hormone Therapy
Status:
RECRUITING
Status Verified Date:
2024-05
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:
This study was planned to evaluate the effect of education on the management of side effects and the use of cooling pillowcase on hot flush complaints sleep and quality of life in women with breast cancer receiving hormone therapy
Detailed Description:
It is planned to apply pre-test evaluations in the 1st week and post-test evaluations in the 9th week to the intervention training group consisting of women with breast cancer who agree to participate in the study A total of 3 follow-ups will be performed on the patients in the intervention education group in weeks 3 and 7 by telephone interview method and in week 5 by face-to-face interview method using the Patient Follow-up Form In addition in order to evaluate the effectiveness of the education given to the patients in the intervention education group the Practices for Coping with the Side Effects of Hormone Therapy Form will be completed in the 5th and 9th weeks
The control group consisting of women with breast cancer who agreed to participate in the study will be administered pre-test evaluations at week 1 and post-test evaluations at week 9 The patients in the control group will not be subjected to any intervention by the researcher their routine treatment and care will continue and they will be followed up only once in the 5th week by phone call
The control group consisting of women with breast cancer who agreed to participate in the study will be administered pre-test evaluations at week 1 and post-test evaluations at week 9 The patients in the control group will not be subjected to any intervention by the researcher their routine treatment and care will continue and they will be followed up only once in the 5th week by phone call
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