Only healthy participants aged 18–45 with a regular menstrual cycle are included. Potential existing (pre-)menstrual symptoms are assessed.
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: • Legal adulthood • Menstrual cycle length between 21 and 35 days • Individuals with a natural menstrual cycle who are not taking any medications that affect hormonal regulation (e.g., contraceptives) • Ability to use a mobile device
Exclusion criteria
Exclusion criteria: • Participation in a course that provided instruction in daily mindfulness practice within the past 6 months • Current pregnancy and/or breastfeeding within the past 3 months
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary endpoint is: Does mindfulness increase to a greater extent in the intervention group compared to the active control group and the waitlist control group? This will be assessed using the following online questionnaire: • Mindfulness: Five Facet Mindfulness Questionnaire (FFMQ-D) (Michalak et al., 2016). | — |
Secondary
| Measure | Time frame |
|---|---|
| The secondary endpoints comprise changes in body awareness, psychological well-being, quality of life, positive and negative menstrual changes, and coping with these changes, which will be evaluated using the following online questionnaires: • Questions on participants’ menstrual cycle: based on the Reproductive Status Questionnaire (RSQ) by Schmalenberger et al. (2021). • Premenstrual symptoms: screening of positive and negative premenstrual changes, following Kues et al. (2018). • Coping with premenstrual changes: Premenstrual Change Coping Inventory (PMS-Cope) (Kaiser et al., 2018). • Psychological well-being: WHO-5 (Brähler et al., 2007). • Life satisfaction: Short Scale of Life Satisfaction-1 (Beierlein et al., 2014). • Interoceptive awareness: Multidimensional Assessment of Interoceptive Awareness (MAIA) (Mehling et al., 2018). | — |
Countries
Germany