Correlations among Core Outcomes in Menopause-recommended vasomotor symptom outcomes in MsFLASH trials
- PMID: 37963308
- PMCID: PMC10756428
- DOI: 10.1097/GME.0000000000002280
Correlations among Core Outcomes in Menopause-recommended vasomotor symptom outcomes in MsFLASH trials
Abstract
Objective: This study aimed to advance understanding of vasomotor symptom (VMS) outcomes measurement using pooled data from three Menopause Strategies Finding Lasting Answers to Symptoms and Health (MsFLASH) trials.
Methods: Participants self-reported VMS frequency, severity, and bother using daily diaries; completed standardized measures of VMS interference, insomnia severity, and sleep quality/disturbance; and completed four treatment satisfaction items. Analyses included descriptive statistics, Pearson correlations (baseline pooled sample, posttreatment pooled sample, posttreatment placebo only), t tests, and analysis of variance.
Results: Participants were mostly postmenopausal (82.9%) and a mean of 54.5 years old. VMS frequency was fairly correlated with severity, bother, and interference for pooled baseline and placebo posttreatment samples ( r values = 0.21-0.39, P values < 0.001) and moderately correlated with severity, bother, and interference for pooled posttreatment ( r values = 0.40-0.44, P values < 0.001). VMS severity, bother, and interference were moderately correlated ( r values = 0.37-0.48, P values < 0.001), with one exception. VMS severity and bother were strongly correlated ( r values = 0.90-0.92, P values < 0.001). VMS interference was moderately correlated with insomnia ( r values = 0.45-0.54, P values < 0.001) and fairly to moderately correlated with sleep quality/disturbance ( r values = 0.31-0.44, P values < 0.001). Other VMS outcomes were weakly to fairly correlated with insomnia ( r values = 0.07-0.33, P values < 0.001 to < 0.05) and sleep quality/disturbance ( r values = 0.06-0.26, P values < 0.001 to > 0.05). Greater improvement in VMS and sleep over time was associated with higher treatment satisfaction ( P values < 0.001).
Conclusions: This pooled analysis advances understanding of VMS outcomes measurement and has implications for selecting measures and creating future research.
Copyright © 2023 by The Menopause Society.
Conflict of interest statement
Financial disclosure/conflicts of interest: Dr. Carpenter received past consulting fees from the University of Wisconsin and Simumetrix SMX Health. Dr. Hunter receives funding from TurningPoint Charity and HelloTherapeutics. All other authors have no disclosures.
References
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- U.S. Department of Health and Human Services (DHHS). Estrogen and estrogen/progestin drug products to treat vasomotor symptoms and vulvar and vaginal atrophy symptoms - recommendations for clinical evaluation: Draft guidance January 2003. Rockville: Food and Drug Administration Center for Drug Evaluation and Research (CDER).
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