This pilot study will assess the safety and feasibility of intravenous (IV) ketamine in older adults with Treatment-Resistant Depression (TRD). In addition, this study will develop and utilize innovative methodological approaches to demonstrate the feasibility of precision medicine and mobile health approaches in depression treatment.
Participants in this study will receive ketamine infusions twice a week for 4 weeks (acute phase). Participants who respond or remit will continue with an additional 4 weeks of weekly ketamine infusions (continuation phase). Participants will be assessed at baseline, end of acute phase, and end of continuation phase for effectiveness, safety, and executive functioning. Participants will be asked to complete daily surveys of their depression symptoms during their participation.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
25
ketamine will be infused using an IV infusion pump at a rate of 0.5 mg/kg of body weight over 40 minutes
UCLA Late-Life Mood, Stress, and Wellness Research Program
Los Angeles, California, United States
Washington University School of Medicine Healthy Mind Lab
St Louis, Missouri, United States
Columbia University Adult and Late Life Depression Clinic
New York, New York, United States
UPMC Late-Life Depression, Evaluation, Prevention, and Treatment Program
Pittsburgh, Pennsylvania, United States
Remission From Depression
Remission defined as Montgomery Asberg Depression Rating Scale score ≤10. Scale ranges from 0-60 with higher scores indicating higher depression severity.
Time frame: 4 weeks for acute phase, 8 weeks for continuation phase
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University Health Network
Toronto, Ontario, Canada