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Clinical Trials in Turkey / NCT07657078
Starting soon Not applicable

Meleis' Transition Theory-Based Education and Counseling Program in Menopausal Women

NCT07657078 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2026-06-15
Last updated
2026-06-22

Condition(s) studied

MenopauseMenopausal SymptomsPerimenopausal Depression

Investigational drug(s) / intervention(s)

Meleis' Transition Theory-Based Education and Counseling ProgramStandard Information

Meleis' Transition Theory-Based Education and Counseling Program: The intervention is a structured education and counseling program developed according to Meleis' Transition Theory. The program consists of four weekly group sessions lasting approximately 90 minutes each. Educational content includes menopause and life transitions, facilitators and inhibitors of menopausal transition, physical and psychological effects of menopause, social support systems, coping strategies, and self-management skills. Participants also receive ongoing support through a secure online messaging platform and follow-up counseling sessions.

Standard Information: Participants receive routine care and standard health information available in primary healthcare settings during the study period. After completion of final assessments, participants are offered a one-day educational session.

Study summary

This randomized controlled trial aims to evaluate the effectiveness of a Meleis' Transition Theory-based education and counseling program on menopausal symptoms, perimenopausal depression, and menopause-specific quality of life among naturally menopausal women aged 45 to 55 years.

Participants will be randomly assigned to either the intervention group or the control group. The intervention group will receive a structured four-week education and counseling program based on Meleis' Transition Theory, supported by a secure online messaging group and follow-up counseling sessions. The control group will receive routine care and standard information during the study period and will be offered a one-day educational session after completion of the final assessment.

The outcomes will be measured at baseline and Week 16 using the Menopause Rating Scale, the Perimenopausal Depression Scale, and the Menopause-Specific Quality of Life Questionnaire-II.

Eligibility

Sex
FEMALE
Min age
45 Years
Max age
55 Years
Healthy volunteers
No
Inclusion Criteria: * Female participants aged 45 to 55 years * Naturally menopausal women * Menopause duration not exceeding 2 years * Experiencing menopausal symptoms * Sexually active * Able to read and write Turkish * Willing to participate voluntarily * Able to provide written informed consent * Not currently receiving hormone replacement therapy * No history of psychiatric disorders * No previous menopause-related education Exclusion Criteria: * Failure to continue participation in the study * Failure to attend education and counseling sessions * Withdrawal from the study at any time * Withdrawal of informed consent * Loss to follow-up

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Ankara Medipol University Ankara Turkey (Türkiye)

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07657078 on ClinicalTrials.gov ↗ ← All trials in Turkey