Marco Canevelli1, Matteo Cesari2,3, Flaminia Lucchini1, Martina Valletta1, Michele Sabino1, Eleonora Lacorte4, Nicola Vanacore4, Giuseppe Bruno1. 1. Department of Neurology and Psychiatry, "Sapienza" University of Rome, Rome, Italy. 2. Gérontopôle, Centre Hospitalier Universitaire de Toulouse, Toulouse, France. 3. Université de Toulouse III Paul Sabatier, Toulouse, France. 4. National Centre for Epidemiology, Surveillance, and Health Promotion, National Institute of Health, Rome, Italy.
Abstract
OBJECTIVES: To determine whether neuropsychiatric symptoms (NPSs) are adequately considered in clinical research on Alzheimer's disease (AD). DESIGN: Systematic review. SETTING: Randomized controlled trials (RCTs) recruiting individuals with AD and published during the last 10 years in 16 major general medicine, neurology, psychiatry, and geriatric psychiatry journals and RCTs registered on clinicaltrials.gov and currently enrolling individuals with AD. PARTICIPANTS: Individuals with AD. MEASUREMENTS: Outcome measures adopted by the included studies. RESULTS: Only 21.4% of the included studies identified through the bibliographic searches had measures of NPSs as a primary outcome. Only 17.7% of the studies retrieved on clinicaltrials.gov made a specific effort to test the effect of pharmacological or nonpharmacological interventions on NPSs. CONCLUSION: These findings show how rarely previous and current research on AD has considered NPSs as primary research targets. Although these symptoms are widely recognized as the most-stressful and -challenging manifestations of dementia, they are addressed much less often than other research targets.
OBJECTIVES: To determine whether neuropsychiatric symptoms (NPSs) are adequately considered in clinical research on Alzheimer's disease (AD). DESIGN: Systematic review. SETTING: Randomized controlled trials (RCTs) recruiting individuals with AD and published during the last 10 years in 16 major general medicine, neurology, psychiatry, and geriatric psychiatry journals and RCTs registered on clinicaltrials.gov and currently enrolling individuals with AD. PARTICIPANTS: Individuals with AD. MEASUREMENTS: Outcome measures adopted by the included studies. RESULTS: Only 21.4% of the included studies identified through the bibliographic searches had measures of NPSs as a primary outcome. Only 17.7% of the studies retrieved on clinicaltrials.gov made a specific effort to test the effect of pharmacological or nonpharmacological interventions on NPSs. CONCLUSION: These findings show how rarely previous and current research on AD has considered NPSs as primary research targets. Although these symptoms are widely recognized as the most-stressful and -challenging manifestations of dementia, they are addressed much less often than other research targets.