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Clinical Trial Summary

A recent systematic review suggested that symptom monitoring can result in reductions in menopausal symptoms and improvements in health-related behaviours. To date, no studies have experimentally investigated whether symptom monitoring could be beneficial as an intervention for menopausal women. One hundred menopausal women were randomised into either a Monitoring-intervention or Control group. A mixed between/ within design was employed, with group membership (i.e., Monitoring-intervention or Control) as the between-subjects component, and time (i.e., baseline and 2-weeks follow-up) as the within-subjects component. Dependent variables included symptom reductions and emotional reactions. Secondary outcomes included help-seeking, communication, medical decision-making, health awareness, self-efficacy, and health anxiety.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05603234
Study type Interventional
Source University of South Wales
Contact
Status Completed
Phase N/A
Start date March 14, 2021
Completion date October 14, 2021

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