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The study will be conducted in two groups as guided imagery and control. Participants will be approached at the Public Education Center. After perimenopausal women are evaluated according to eligibility criteria, those who are eligible will be informed about the research and written informed consent will be obtained from those who agree. Random assignment of women to the study groups will be carried out using randomization.
Enrollment
Sex
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Volunteers
Inclusion criteria
Being between 45-59 years of age
Being in the perimenopausal period according to the Stages of Reproductive Aging Workshop (STRAW) criteria (stage +1 or +2)
Having entered natural menopause in postmenopausal women
Scoring above 10 on the Women's Health Initiative Insomnia Rating Scale
Owning a smartphone
Ability to understand and speak Turkish
No hearing impairment
Volunteering to participate in the study
Exclusion criteria
Primary purpose
Allocation
Interventional model
Masking
68 participants in 2 patient groups
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Central trial contact
Derya Öztürk Özen
Data sourced from clinicaltrials.gov
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