Climactericum

2

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

Condition / disease
Location
Status: Not yet recruiting

The Effect of Cold Packs on Hot Flushes and Depression in Women Going Through the Climacteric Period

This study is planned as a pre-post test, randomised controlled, experimental trial designed to determine the effect of applying a cold gel pack to the Sanyinjiao (SP6) and Hegu (Large Intestinal 4 (LI4)) acupoints on hot flushes and depression in women during the climacteric period.

Participants needed: 80
Trial details
Biological sex: FemaleType: InterventionalSponsor: Rabia AtillaUpdated: Apr 21, 2026Locations: 1
Eligibility criteria

In the perimenopausal phase (no menstruation for 3-11 months or an increase in i... [+3]

Women who have entered menopause following surgery, [+9]

Status: Recruiting

Nursing Interventions to Enhance Positive Mental Health and Self Care in Women During the Climacteric

This study will test whether a nursing program using podcasts and videos can help women feel better and take better care of themselves during the climacteric (the stage leading up to and following menopause). Women between 42 and 58 years old who attend public sexual and reproductive health clinics in the Metropolitan South Health Region of Barcelona (Sant Boi, Sant Feliu, and Cornellà) will be invited to participate. Participants will be randomly assigned to one of two groups: Intervention Group: will receive access to podcasts and videos offering practical advice and strategies to improve emotional well-being and self-care. Control Group: will receive standard care. All participants will complete questionnaires before and after the program to assess symptoms, mental health, and satisfaction with self-care. Statistical methods will be used to compare the results between both groups and determine whether the program produces a significant difference. The aim of the study is to demonstrate that this digital nursing intervention is effective and could be implemented more broadly in healthcare settings.

Participants needed: 250
Trial details
Age: 42-58Biological sex: FemaleType: InterventionalSponsor: University of BarcelonaUpdated: Feb 5, 2026Locations: 1
Eligibility criteria

Women aged 42-58 years attending the participating ASSIR centers. [+1]

Cognitive or learning impairments preventing comprehension of study procedures. [+4]