---
title: Adapting and Piloting Acceptance and Commitment Th | PMS & PMDD trial
description: Running, not recruiting. Clinical trial on Premenstrual Dysphoric Disorder and Premenstrual Exacerbation of Mood Disorder run by Women's College Hospital in C
url: https://niyora.com/research/trials/adapting-and-piloting-acceptance-and-commitment-therapy-act-nct06462391/
---

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- Adapting and Piloting Acceptance and Commitment Therapy (ACT) for Severe Premenstrual Mood Symptoms

Running, not recruiting

# ACT-PM: Adapting and Piloting Acceptance and Commitment Therapy (ACT) for Severe Premenstrual Mood Symptoms

Adapting and Piloting Acceptance and Commitment Therapy (ACT) for Severe Premenstrual Mood Symptoms: An Open-label Feasibility Study of ACT-PM

Status Running, not recruiting Registry ID NCT06462391 Type Interventional (tests a treatment) Phase NA Conditions Premenstrual Dysphoric Disorder, Premenstrual Exacerbation of Mood Disorder What is tested Acceptance and Commitment Therapy (ACT) Group (behavioral) Sponsor Women's College Hospital Where Canada Participants 50 (planned) Start 2024-12-01 Completion 2026-12-31 Last update 2025-12-22

## About the study

In the weeks prior to menstruation, many individuals experience mood and physical symptoms that negatively impact their quality of life and functioning. Approximately 5% of women and menstruating individuals have such severe symptoms that they meet criteria for Premenstrual Dysphoric Disorder (PMDD). Further, of those with underlying mood disorders (i.e., depression, bipolar disorder) about 60% have cyclical worsening of symptoms classified as premenstrual exacerbation (PME). Both PMDD and PME are associated with significant impairment, yet limited effective options exist to treat these conditions. In this project, the investigators will adapt and evaluate an Acceptance and Commitment Therapy (ACT) group for PMDD and PME, entitled ACT-Premenstrual (ACT-PM), delivered virtually to maximize accessibility. The investigators will examine whether ACT-PM is feasible to deliver and whether it is acceptable to group participants and those facilitating the group. The study will lay the groundwork for future research to determine if the group is effective. If effective, the intervention could be scaled up to improve quality of life and outcomes for individuals suffering from PMDD and PME.

Summary from ClinicalTrials.gov.

[See the full record](https://clinicaltrials.gov/study/NCT06462391)

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