Skip to content

Journaling on quality of life and menopausal symptoms

The effect of journaling on menopausal symptom severity and quality of life in women during menopausal transition: A Randomized Clinical Trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20250803066737N1
Enrollment
150
Registered
2025-09-18
Start date
2025-08-22
Completion date
Unknown
Last updated
2025-10-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

menopausal symptoms.

Interventions

Intervention 1: Intervention group:This group will perform combined guided and reflective-emotional journaling for four weeks, for 15 to 20 minutes daily. Participants will receive a structured physic

Sponsors

Gonabad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
45 Years to 55 Years

Inclusion criteria

Inclusion criteria: Iranian women aged 45-55 who are in the menopausal transition Minimum education level of a high school diploma (to ensure the ability to keep daily diaries) Providing informed consent to participate in the study Having mild to moderate menopausal symptoms (based on the Menopause Rating Scale)

Exclusion criteria

Exclusion criteria: history of psychiatric disorders (based on participant self-report) history of receiving any psychological treatment or psychiatric intervention in the last 6 months history of experiencing a major stressful life event in the last 6 month history of using hormonal medications effective on menopausal symptoms in the last 6 months (based on participant self-report) history of using non-hormonal medications effective on menopausal symptoms in the last 6 months (based on participant self-report) history of severe chronic disease (based on participant self-report and, if needed, confirmation of medical records or referral to a physician) history of using smoking and alcohol consumption in the last 6 months (based on participant self-report) history of hysterectomy and oophorectomy

Design outcomes

Primary

MeasureTime frame
Severity of menopausal symptoms. Timepoint: At the beginning of the study (pre-test), immediately after the four-week intervention, and two months after the intervention is completed. Method of measurement: Menopause Rating Scale (MRS).;Menopause-specific quality of life. Timepoint: At the beginning of the study (pre-test), immediately after the four-week intervention, and two months after the intervention is completed. Method of measurement: Menopause-Specific Quality of Life Questionnaire (MENQOL).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSamane Tavakoli

Gonabad University of Medical Sciences

stmidwife97@gmail.com+98 51 5722 3028

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026