Menopausal Depression

4

Review clinical trials related to Menopausal Depression. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Sleep and Light Intervention (SALI) for Menopausal Mood Dysfunction

The goal of this clinical trial is to learn more about mood, sleep, and activity during menopause. The main question it aims to answer is: can mood and sleep dysfunction in menopause be improved by resetting misaligned circadian rhythm through one night of strategic sleep timing adjustment and two weeks of exposure to bright light at a certain time of day? Researchers will compare sleep timing (earlier vs. later) and bright white light exposure (morning or evening) to investigate the effect of melatonin levels on mood, sleep, and activity. Participants will 1) submit urine samples to measure melatonin levels, 2) be assigned to advance or delay their sleep for one night, 3) sit in front of a light box for 30 minutes per day (morning or evening) for 14 days, 4) complete questionnaires about their mood and sleep, and 5) wear a device that will measure their activity.

Participants needed: 120
Trial details
Age: 18+Biological sex: FemaleType: InterventionalSponsor: University of California, San DiegoUpdated: Feb 27, 2026Locations: 1
Eligibility criteria

Perimenopausal women with irregular menstrual cycles for at least 3 months [+2]

Actively suicidal or psychotic [+4]

Status: Not yet recruiting

Interest of Adaptated Physical Activity (APA) on the K Recovery Constant, Reflecting the Rate of Muscle Oxygenation Recovery in Menopausal Women Suffering From Depression

APhyDeM is a randomized controlled study investigating the relationship between adapted physical activity and mitochondrial function in postmenopausal women with major depressive disorder. Depression is associated with metabolic dysfunction, including alterations in mitochondrial activity and inflammatory processes. Physical activity has been shown to influence mitochondrial function, yet individuals with depression frequently experience reduced physical activity levels. This study aims to evaluate whether an adapted physical activity program can improve mitochondrial function compared with a control intervention. Mitochondrial function will be indirectly assessed using near-infrared spectroscopy to measure post-exercise muscle oxygen recovery kinetics. The study compares adapted physical activity with a non-physical therapeutic intervention in postmenopausal women receiving care in a psychiatric day hospital setting.

Participants needed: 52
Trial details
Age: 40+Biological sex: FemaleType: InterventionalSponsor: Centre Hospitalier Universitaire de BesanconUpdated: Feb 18, 2026Locations: 1
Eligibility criteria

Menopaused women aged ≥ 40 years old, [+3]

Medical contraindication for physical activity (cardio-vascular pathology, and/o... [+2]

Status: Not yet recruiting

Transcranial Electrical Stimulation for Noninvasive Study of Menopausal/Perimenopausal Symptoms

Participants are being invited to a research study. This research aims to assess the tolerability of transcranial electrical stimulation of the brain, and explore the response of TES on menopausal/perimenopausal symptoms including hot flashes effects, depression/anxiety, memory-problems, and muscular problems. This study will assess what types of electrical brain stimulation affect different menopausal related symptoms. This study will help guide the development of electrical stimulation to be used for improving women's health during menopause transition.

Participants needed: 50
Trial details
Age: 40-60Biological sex: FemaleType: InterventionalSponsor: Carnegie Mellon UniversityUpdated: Jan 29, 2026
Eligibility criteria

Age between 40 and 60 years [+6]

Disorders that may mask or coincide with menopause and peri-menopause, such as:... [+3]

Status: Recruiting

A Trial to Investigate the Accuracy of a Wearable Device in Collecting Data Related to Perimenopausal Symptoms in Women

The goal of this observational study is to investigate the accuracy of the device in characterizing perimenopausal and menopausal symptoms including vasomotor symptoms, anxiety, sleep quality compared to self-reported symptoms via an app. The main question it aims to answer is: What is the accuracy of the developed algorithm from the investigational device compared to daily self-report via an app in characterizing perimenopausal symptoms? Participants will be asked to wear IndentifyHer's wearable non-invasive sensor and complete a daily electronic diary and questionnaires on stress, anxiety, and sleep.

Participants needed: 110
Trial details
Age: 35-55Biological sex: FemaleType: ObservationalSponsor: IdentifyHer LimitedUpdated: Sep 18, 2025Locations: 1
Eligibility criteria

Females between 35-55 years of age, inclusive [+9]

Allergy or sensitivity to adhesive used for wearing the investigational device [+11]