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NCT05191108: PMS and MSRP

Premenstrual Syndrome (PMS) and Mindfulness Stress Reduction Program (MSRP)

Completed NA Last updated 9 June 2022
What this trial tests

NA trial testing mindfulness stres reduction programe in Premenstrual Syndrome in 74 participants. Completed in 30 April 2022.

Timeline
21 February 2022
Primary endpoint
21 April 2022
30 April 2022

Quick facts

Lead sponsorNURDİLAN SENER
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposeprevention
Enrollment74
Start date21 February 2022
Primary completion21 April 2022
Estimated completion30 April 2022
Sites2 locations across Turkey (Türkiye)

Drugs / interventions tested

Conditions studied

Sponsor

NURDİLAN SENER

Who can join

Adults 17 to 30, female only, with Premenstrual Syndrome. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Premenstrual syndrome (PMS) is a disorder characterized by emotional, physical and behavioral symptoms that increase the severity of the menstrual cycle in women of reproductive age during the luteal phase and disappear spontaneously a few days after the onset of menstruation. Nonpharmacological applications are often preferred to reduce premenstrual symptoms. It has been stated that with the meditation practices of mindfulness, individuals experience less anxiety, depression, anger and lower levels of psychological distress, including anxiety. . It is thought that the mindfulness stress reduction program can reduce the symptoms of PMS by regulating the stress level and emotional balance of women.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. The Effect of a Mindfulness-Based Stress Reduction Program on Premenstrual Symptoms: A Randomized Controlled Trial.
    Şener Çetin N, Şolt Kırca A. · · 2023 · cited 5× · PMID 37335817 · DOI 10.1111/jmwh.13530

Verify or expand the search:

Other recruiting trials for Premenstrual Syndrome

Currently open trials in the same condition.

Other NURDİLAN SENER trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05191108.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing