Viewing Study NCT06583629



Ignite Creation Date: 2024-10-25 @ 7:49 PM
Last Modification Date: 2024-10-26 @ 3:39 PM
Study NCT ID: NCT06583629
Status: COMPLETED
Last Update Posted: None
First Post: 2024-08-28

Brief Title: Effect of Emotion Freedom Technique on Perceived Stress Resilience and Sexual Satisfaction Among Women After Mastectomy
Sponsor: None
Organization: None

Study Overview

Official Title: Effect of Emotion Freedom Technique on Perceived Stress Resilience and Sexual Satisfaction Among Women After Mastectomy
Status: COMPLETED
Status Verified Date: 2024-08
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: A quasi-experimental design was utilized involving a convenient sample of 112 Egyptian mastectomized women Data were collected and analyzed to determine the correlations between the variables of interest
Detailed Description: Aim of the Study

This study set out to evaluate the effect of emotion freedom technique on perceived stress Resilience and sexual satisfaction among women after mastectomy

Setting and study design

The study was conducted in the surgical department Beni-Suef University Hospital at Beni-Suef Governorate Egypt A quasi-experimental design was utilized to carry out the study

Participants

A total of 112 Egyptian women who had undergone mastectomy were recruited based on the following inclusion criteria a absence of any psychiatric diagnoses b no prior exposure to courses on emotional freedom techniques c no chronic illnesses and d willingness to participate in the study

Study instruments and measures

For this study a well-structured interview using a previously prepared questionnaire with the participants using the participants mother tongue Arabic was employed The researchers developed the questionnaire incorporating relevant Connor-Davidson Resilience scale items Perceived Stress Scale and the Sexual Satisfaction Index from related studies The instruments were translated from English to Arabic at the Center for Specialized Languages Faculty of Arts Helwan University A panel of experts in psychology psychiatry and psychiatric nursing then evaluated the instruments validity and suitability for use with mastectomized women The questionnaires validity was further confirmed through a pilot study involving 10 participants Then the questionnaire was distributed by the researchers through performing an interview with the participants in the surgical department Beni-Suef University Hospital

This research instrument encompasses four primary sections the first one containing the participants basic and educational information including items such as age educational level place of residence marital status occupation economic status and medical history of the women The second section was Connor-Davidson Resilience Scale CD-RISC which was developed Kathryn and Jonathan 2003 Connor-Davidson Resilience Scale CD-RISC comprises 25 items that measure resilience or capacity to change and cope with adversity Respondents indicated their response on a 5-point Likert scale with higher scores indicating greater resilience Scoring criteria As for the scoring system of the CD-RISC contains 25 items all of which carry a 5-point range of responses as follows not true at all 0 rarely true 1 sometimes true 2 often true 3 and true nearly all of the time 4 The scale is rated based on how the subject has felt over the past month The total score ranges from 0-100 with higher scores reflecting greater resilience Cronbachs alpha coefficient for the full scale was 089

The third research instruments part was the Perceived Stress Scale PSS-10 which was developed by Cohen and colleagues 1983 The Perceived Stress Scale PSS is widely considered the gold standard instrument for measuring stress perception This questionnaire is used to assess the degree to which a respondent finds circumstances in their life to be unpredictable uncontrollable andor overwhelming Questions on the PSS ask the respondent to rate their feelings and thoughts for the past month indicating that a relatively recent time frame is assessed PSS designed to measure the degree to which situations in ones life are appraised as stressful This version of the PPS had 10 items four positive items items 4 5 7 8 and six negative items items 1 2 3 6 9 and 10 Each item is scored on a 5-point scale ranging from 0 never to 4 very often The positive elements ratings are reversed for example 04 13 22 etc and then summing across all 10 items a higher score indicates more perceived stress We evaluated the internal consistency of the questionnaire with Cronbachs alpha resulting in a satisfactory value of 082

The fourth part of the research instrument was the Sexual Satisfaction Index SSI which was developed by Leth-Nissen and colleagues 2021 There were nine items in this edition of the SSI five positive items items 1 2 3 8 and 9 and four negative ones items 4 5 6 and 7 Every item is scored on a 5-point rating system with the negative ratings being reversed and ranging from 1 strongly disagree to 5 strongly agree The SSIs total score falls between 1 and 45 A greater level of sexual satisfaction is indicated by a higher sum score Estimates of internal reliability for the SSI produced acceptable Cronbachs alpha coefficients to the full scale 088

Procedures

The data collection for this study was instituted after obtaining the ethical approval from the faculty of medicine at Beni-Suef University followed by the approval from the hospital authorities to conduct the current study after an explanation of the aim of the study

The researchers prepared the research instruments after reviewing related articles and periodicals The instrument was translated from English to the participants mother tongue Arabic at the Center for Specialized Languages of the Faculty of Arts Helwan University A panel of experts in psychology psychiatry and psychiatricmental health nursing then evaluated the instruments validity and suitability for use with nursing students

The survey was successfully conducted with participants in the hospital in the form of a well-structured interview where the researchers met the participants explained the aim of the study to them assessed their ability to participate and obtained their written informed consent the informed consent explaining the studys aim confidentiality guarantees and the ability to withdraw from the study at any time without any fear Then the data was collected The emotional freedom technique was applied through various phases The preparatory phase involved reviewing the studies and available literature related to the research problem and theoretical knowledge using evidence-based articles textbooks internet periodicals and journals The assessment phase in which the researchers communicated with the accountable nursing supervisors in the surgical department daily to find out how many patients were recently admitted to the surgical department and if they fulfilled the inclusion criteria The researchers clarified the nature and the aim of the study to all participants who were involved in the study after taking their written approval of participation The researchers interviewed the participants pre-the emotional freedom technique interventions to complete the socio-demographic perceived stress resilience and sexual satisfaction The interview lasted between 25 and 35 minutes

Planning Phase Development of Emotional Freedom Technique Interventions The objectives were formulated with careful consideration of the needs of the women involved drawing on recent significant research and expert validation from the nursing field These objectives were revised and refined based on expert feedback to ensure they could be applied in various ways One such approach included the creation of a booklet which highlighted the key aspects of the emotional freedom technique specifically for women who had undergone mastectomies The booklet designed by researchers was written in simple Arabic and accompanied by illustrative photos Implementation phase The implementation of emotional freedom technique interventions was carried out by the researchers Interventions were provided three times per week The emotional freedom technique with approximately 55 minutes included theoretical information about breast cancer signs and symptoms treatment and its effect on stress resilience and sexual satisfaction 25 minutes and steps of applying the emotional freedom technique 30 minutes The evaluation phase aimed to reevaluate the participants to find any variations in their baseline response level following the intervention phase Both before and after using the emotional freedom technique the researchers assessed participants perceived stress resilience and sexual satisfaction twice The same tools were used by the researchers to compare them and investigate any notable differences in the results

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None