Menopause
Conditions
Keywords
Climacteric, Education, Mental health, Menopause
Brief summary
The aim of the study is to investigate if group education about the topic menopause to women in PHC can improve women's menopausal symptoms and reduce depression.
Detailed description
One hundred twenty women will be included in the study. The survey population consists of Swedish-speaking women aged 45-55 years and seek care at Distriktsköterskemottagningen in Skene and at the Antenatal clinic in Svenljunga. The selection is done consecutively. Method: Grouping:The women will be randomly allocated to intervention group and control group (60/60). The intervention: The project includes the implementation of a total of four equivalent group treatments. Two of the group education will be at Skene Medical center and two Svenljunga Medical center. Group treatments are carried out by the district nurse and midwife in common. Each treatment group includes 15 women. A total of 60 women will thus participate in group education..Each treatment group consists of two information sessions of 2 hours. The first information contains information about the menstrual cycle, hormonal shift, urogenital symptoms, and information on prevention and health promotion self-care. The other information currently contains information about cardiovascular risk factors during menopause, relations, mental health, information about depressive symptoms and for preventive measures and health-promoting self-care. The control group did not obtain any group education or any other intervention.
Interventions
OTHERGroup education
Intervention involving two education session with topics common in menopause transition.
Sponsors
Vastra Gotaland Region
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
FEMALE
Age
45 Years to 55 Years
Healthy volunteers
Yes
Inclusion criteria
* female gender, 45 to 55 years of age, comprehension and fluency in the Swedish language.
Exclusion criteria
* that the patient did not any longer want to participate in the study.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Change in menopause symptoms during baseline to four month follow up. The measurement that be used were The Menopause Rating Scale (MRS). | from baseline to four month follow up | Primary outcome measure: Change in menopausal symptoms (using the menopause rating scale). |
| Change in depression symptoms during baseline to four month follow up. The measurement that be used was The Montgomery-Asberg Depression Rating Scale (MADRS). | from baseline to four month follow up | Primary outcome measure: Change in depression score (using the Montgomery-Asberg depression rating scale) |
Outcome results
None listed