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) — BEHAVIORAL
    Mind-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 retraining
    Participants receive immediate access to the 12-week Amygdala and Insula Retraining (AIR) program in addition to treatment as usual.
  • No Intervention: Control
    Participants 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)

FacilityCityStateZIPSite coordinators
Luther College Department of PsychologyDecorahIowa52101-

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