Memantine Treatment for Improving Rehabilitation Outcomes and Preventing Depression in Older Adults

Eric Lenze35 enrolled

Overview

This study will evaluate the effectiveness of memantine in improving rehabilitation outcomes and preventing major depressive disorder in older adults who have been admitted to a rehabilitation hospital for a hip fracture or cardiopulmonary condition.

Depression is a serious medical illness that is often difficult to diagnose and treat. It occurs in people of all ages, but is often overlooked in older adults. Depression frequently co-occurs with other serious illnesses, and may be mistaken by both patients and health care givers as a normal consequence of the illness. However, these misconceptions toward depression contribute to the underdiagnosis and undertreatment of depressive disorders in older people. In turn, depression may hinder a patient's recovery from an illness. This study will evaluate the effectiveness of memantine in improving rehabilitation outcomes and preventing major depressive disorder in older adults who have been admitted to a rehabilitation hospital for a hip fracture or a cardiopulmonary condition. This double-blind study will last for 12 months. Participants will be randomly assigned to receive either placebo or memantine, which is a drug that is often used to treat Alzheimer's disease. Both memantine and placebo will be administered to participants for 12 weeks. All participants will be followed for an additional 40 weeks. Outcome measurements will include participants' depressive symptoms, motivation, and learned helplessness. In addition, medication side effects, functional outcome, and incidence of major depressive disorder will be measured. All measurements will be taken at Week 12 and Month 12.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

QUADRUPLE

Enrollment

Conditions

Depression

Interventions

MemantineDRUG

Memantine dosage is started at 10 mg daily and is increased at Week 1 as tolerated to 10 mg two times a day.

PlaceboOTHER

Placebo distribution is planned to mimic the active drug.

Eligibility

Sex: ALLMin age: 60 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Admission to a skilled nursing facility for rehabilitation within 3 months of recent disabling medical event (e.g., hip fracture) * Medically stable (e.g., no active seizures, delirium, unstable pulse/blood pressure) Exclusion Criteria: * Aphasia or cognitive impairments sufficiently severe to prevent valid assessment (e.g., a score of less than 22 on the Mini Mental State Examination) * Current major depressive episode * History of or current psychosis or mania * Current substance or alcohol abuse or dependence (within 3 months of study entry) * Current use of memantine * Sensitivity or contraindication to memantine * End-stage kidney, liver, heart, or lung disease * Recent hemorrhagic stroke * A FIM score of greater than 70 (on a 91 point scale)

Locations (1)

University of Pittsburgh Medical Center

Pittsburgh, Pennsylvania, United States

Outcomes

Primary Outcomes

Depressive Symptoms

Hamilton depression rating scale ; scale ranges 0 (no symptoms) to 52 (severe depression)

Time frame: week 0, week 12

Secondary Outcomes

Incidence of Major Depressive Disorder

cumulative incidence over 12 weeks of follow-up

Time frame: week 12

Functional Recovery

Functional Independence Msure, 13-item motor subscale (scale ranges 13-91, higher scores = better function)

Time frame: week 0, week 12

Data from ClinicalTrials.gov

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