The Effect of Nursing Support Program for Women in Surgical Menopause on Their Life Quality
NCT ID: NCT05809960
Last Updated: 2023-04-12
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
77 participants
INTERVENTIONAL
2020-01-20
2021-07-30
Brief Summary
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Design: The study was a single-center, randomized, controlled trial. Setting: This study was carried out in the gynecology clinic of a training and research hospital in Türkiye.
Method: The participants were randomized into two equal groups: intervention and control. The nursing support program developed in addition to routine nursing care was applied to the intervention group. Routine nursing care was given to the women in the control group. Data were collected with "Personal Information Form", "Menopause-Specific Quality of Life Questionnare", "Pittsburgh Sleep Quality Index" and "Perimenopausal Depression Scale".
Hypothesis:
H0-a: Nursing support program developed in line with the Roy Adaptation Model has no effect on the quality of life of women who have undergone surgical menopause.
H0-b: Nursing support program developed in line with the Roy Adaptation Model has no effect on the sleep quality of women who have undergone surgical menopause.
H0-c: Nursing support program developed in line with the Roy Adaptation Model has no effect on the depressive symptom status of women who have undergone surgical menopause.
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
NONE
Study Groups
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Investigation Group
Education was given, which was prepared in line with the Roy Adaptation Theory and considering the literature, including the problems experienced in menopausal periods and the approaches used to cope with them. The progressive relaxation exercise was explained and taught to the women and the first application was provided with the instructions. "Menopause and Life" booklet prepared in line with Roy Adaptation Theory was given to support the education given and to remember the information afterwards.
Nursing support program
It was discussed about the operation and surgical menopause that the woman will undergo after hospitalization for the operation. Education was given including the problems experienced during menopause and the approaches used to cope with them. Progressive relaxation exercises were taught and practiced. In order to carry out these procedures, an interview of approximately 45-60 minutes was held with each woman. During the program, four planned meetings were held. One of them was face-to-face and the others were phone calls. During the phone calls, the symptoms experienced by the women and their coping methods were discussed and the questions of the women were answered. The average of each phone call was 20-30 minutes.
Control Group
Routine nursing care was given to the control group. The clinical routine has not been exceeded.
Routine nursing care
Routine nursing care was given to the control group. The clinical routine has not been exceeded. It includes discharge training for the surgery.
Interventions
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Nursing support program
It was discussed about the operation and surgical menopause that the woman will undergo after hospitalization for the operation. Education was given including the problems experienced during menopause and the approaches used to cope with them. Progressive relaxation exercises were taught and practiced. In order to carry out these procedures, an interview of approximately 45-60 minutes was held with each woman. During the program, four planned meetings were held. One of them was face-to-face and the others were phone calls. During the phone calls, the symptoms experienced by the women and their coping methods were discussed and the questions of the women were answered. The average of each phone call was 20-30 minutes.
Routine nursing care
Routine nursing care was given to the control group. The clinical routine has not been exceeded. It includes discharge training for the surgery.
Eligibility Criteria
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Inclusion Criteria
* To be literate
* To agree to participate in the study
Exclusion Criteria
* To have an oncological disease
* To have a psychiatric disease
* To use sleeping pills
* To use hormonal therapy
* To have physical and mental disability
* To have barrier to communication
18 Years
FEMALE
Yes
Sponsors
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Mehtap Gümüşay
OTHER
Responsible Party
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Mehtap Gümüşay
Principal Investigator
Locations
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Ordu University
Ordu, , Turkey (Türkiye)
Countries
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Other Identifiers
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OrduU-SBF-MG-1
Identifier Type: -
Identifier Source: org_study_id
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