Occupational Disruption and Role Strain During Perimenopause (NCT07570732)
Occupational Disruption and Role Strain During Perimenopause: A Mixed-Methods Study
🩺 Plain-English Summary (8th-Grade Level)
The purpose of this sequential exploratory mixed-methods study is to examine the relationship between perimenopausal symptom severity and occupational performance, occupational balance, and role participation in women aged 40-55. A secondary purpose is to explore the lived experience of occupational disruption during perimenopause through qualitative interviews.
Who can join: Review the eligibility criteria below.
Location: Russell Sage College — Troy, New York
Age range: 40 Years to 55 Years
🧪 Interventions in This Study
- Confidential Surveys (OTHER)
📋 "Do I Qualify?" — 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria ↗
📍 All Participating Trial Locations (1 Sites)
- Russell Sage College — Troy, New York
📞 Contact the Study Coordinator
Phone: (518) 210-5086
Email: mullic@sage.edu
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
💰 Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
More studies in Perimenopause
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- Evaluation of the Effects of Lifestyle Medicine and Mindfulness-based Group Medical Visits on Stress, Microbiome, and Quality of Life in Women Experiencing Perimenopause and Menopause — Columbus, Ohio
- Shatavari Root Extract for Perimenopausal Symptoms — San Francisco, California
- Amygdala Insula Retraining in the Management of Perimenopause Symptoms — Decorah, Iowa
- Melatonin Effects on Cardiovascular Disease Mechanisms in Midlife Women: A Randomized Clinical Trial — Rochester, Minnesota
Explore by condition: All Perimenopause clinical trials
💡 How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.