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Clinical Trials/NCT06110832
NCT06110832
Completed
Not Applicable

The Effect of Mindfulness-based Yoga and Meditation Practices on Stress, Self-esteem, Body Image and Sexual Adjustment in Breast Cancer Patients Undergoing Modified Radical Mastectomy: A Randomized Controlled Trial

Kutahya Health Sciences University1 site in 1 country41 target enrollmentMay 11, 2023
ConditionsBreast Cancer

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Breast Cancer
Sponsor
Kutahya Health Sciences University
Enrollment
41
Locations
1
Primary Endpoint
Perceived Stress Scale
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

The purpose of this study was to evaluate the effect of mindfulness-based meditation and yoga on stress, self-esteem, body image and sexual adjustment in breast cancer patients.

Detailed Description

The study was conducted in a single-center, prospective (pretest-posttest-2. month follow-up), two-arm (1:1), randomized controlled experimental design. In this study, the effects of an 8-week structured mindfulness-based meditation and yoga program on stress, self-esteem, body image and sexual adjustment will be evaluated in women undergoing modified radical mastectomy. The 8-week interventions were conducted by the researcher. The researcher who performed these applications has a certificate of mindfulness meditation, yoga, breathing and movement trainer. Due to the nature of the research, the researcher is involved in the implementation of the mindfulness-based meditation and yoga program, data collection and data entry into the system. At the same time, the women in the experimental group had to be informed about the research. Therefore, researcher and participant blinding could not be performed. However, randomization was performed to prevent selection bias (1:1). The randomization process was performed by a statistical expert other than the researcher and communicated to the researcher. The participants included in the study were numbered from 1 to 41, preserving their random order in the list received from the hospital. The groups were divided into Group 1 and Group 2 by the statistician and the first group was determined as the experimental group and the second group as the control group by lottery method. The randomization table was created by making use of "http://calculatorsoup.com". Before the 8-week process started, 3 measurements were made to the participants: pre-test, post-test at the end of 8 weeks and follow-up measurement 2 months after the application.

Registry
clinicaltrials.gov
Start Date
May 11, 2023
End Date
December 31, 2023
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Sponsor
Kutahya Health Sciences University
Responsible Party
Principal Investigator
Principal Investigator

Melike Pehlivan

Lecturer

Kutahya Health Sciences University

Eligibility Criteria

Inclusion Criteria

  • Able to read and write Turkish,
  • Who have undergone modified radical mastectomy surgery,
  • Female patients between the ages of 30-55,
  • Premenopausal patients,
  • At least 3 months have passed since the mastectomy operation and all available treatments (chemotherapy and/or radiotherapy treatments),
  • No condition that constitutes an obstacle for active sexual life (for sexual compatibility assessment),
  • Those who have not undergone plastic and reconstructive surgery for the breast after modified radical mastectomy,
  • Those who have no previous meditation and/or yoga experience,
  • Those who do not have a diagnosis of a mental disorder of organic origin,
  • Those who do not have substance and/or alcohol addiction,

Exclusion Criteria

  • Patients who received neoadjuvant chemotherapy in the preoperative period,
  • Patients under the age of 30 and over the age of 55,
  • Patients who have undergone oncoplastic, breast-conserving surgery,
  • Patients with previous experience of mindfulness, meditation or yoga will not be included in the study.

Outcomes

Primary Outcomes

Perceived Stress Scale

Time Frame: Week 1 (pre-test), Week 8 (final test) and 2nd month (follow-up measurement)

The Perceived Stress Scale developed by Cohen, Kamarck and Mermelstein (1983) consists of 14 items and has 2 sub-dimensions (perception of inadequate self-efficacy and perception of stress/discomfort). Individuals are asked to rate on a 5-point Likert scale how often they have experienced certain feelings or thoughts in the last month.

Secondary Outcomes

  • Rosenberg Self-Esteem Scale(Week 1 (pre-test), Week 8 (final test) and 2nd month (follow-up measurement))
  • Sexual Compliance and Body Image Scale(Week 1 (pre-test), Week 8 (final test) and 2nd month (follow-up measurement))
  • Female Sexual Function Scale(Week 1 (pre-test), Week 8 (final test) and 2nd month (follow-up measurement))

Study Sites (1)

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