Amygdala Insula Retraining in the Management of Perimenopause Symptoms
Part of paid clinical trials in Decorah, Iowa.
- Sponsor
- Chronic Conditions Research Fund
- Study ID
- NCT07427459
- Status
- Not Yet Recruiting
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Conditions
Eligibility Criteria
- Sex
- FEMALE
- Age
- 38 Years - 61 Years
- Healthy Volunteers
- Not accepted
Interventions
- Amygdala and Insula Retraining (AIR) — BEHAVIORALMind-body brain retraining intervention
Study Details
The goal of this study is to evaluate a neuroplasticity-based mind-body intervention, Amygdala and Insula Retraining (AIR), compared to a wait-list control in individuals experiencing perimenopausal symptoms. Our research questions include: Does AIR reduce overall perimenopausal symptom burden compared to a wait-list control? Does AIR improve sleep disturbance, vasomotor symptom interference, fatigue, mood, anxiety, and quality of life in perimenopausal individuals? Are symptom changes associated with improvements in autonomic regulation and sleep parameters, as reflected by exploratory wearable measures including heart rate variability?
Key Dates
- Start date
- Mar 1, 2026
- Status verified
- Feb 2026
- Primary completion
- Sep 1, 2026
- Completion
- Sep 1, 2026
Study Design
- Enrollment
- 160 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: Amygdala insula retrainingParticipants receive immediate access to the 12-week Amygdala and Insula Retraining (AIR) program in addition to treatment as usual.
- No Intervention: ControlParticipants receive treatment as usual for 12 weeks and are offered access to the Amygdala and Insula Retraining (AIR) program after completion of the primary outcome assessment.
Primary Outcome Measure
Menopause Rating Scale (MRS) Total Score [ Time Frame: Baseline (Week 0) to post-intervention (Week 12) ]
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Luther College Department of Psychology | Decorah | Iowa | 52101 | - |
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