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Apathy clinical trials

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NCT ID: NCT01481558 Completed - Alzheimer's Disease Clinical Trials

Effects of Transcranial Direct Current Stimulation on the Apathy of Alzheimer's Disease

Start date: January 2012
Phase: Phase 2
Study type: Interventional

This is a phase 2 double-blind, randomized, sham-controlled study to investigate the effects of repeated transcranial direct current stimulation for the treatment of apathy in moderate Alzheimer's Disease in patients selected from an outpatient clinics in São Paulo, Brazil.

NCT ID: NCT01172145 Completed - Alzheimer's Disease Clinical Trials

Treatment of Apathy in Alzheimer's Disease With Modafinil

Start date: July 2005
Phase: Phase 3
Study type: Interventional

This study examined the effects of modafinil on apathetic symptomatology, performance of activities of daily living (ADLs) and caregiver burden in individuals with Alzheimer's disease (AD).

NCT ID: NCT01117181 Completed - Alzheimer's Disease Clinical Trials

Apathy in Dementia Methylphenidate Trial (ADMET)

ADMET
Start date: June 2010
Phase: Phase 2
Study type: Interventional

The Apathy in Dementia Methylphenidate Trial (ADMET) is a masked, placebo-controlled trial that will examine the efficacy and safety of methylphenidate for the treatment of clinically significant apathy in patients with Alzheimer's dementia.

NCT ID: NCT00844090 Completed - Diabetes Clinical Trials

The Role of Apathy in Glycemic Control

Start date: July 2009
Phase: N/A
Study type: Interventional

In spite of several new medications and insulins for the control of blood sugars in patients with diabetes, a large number of patients do not have good control. This likely due to inability to carry out regular activities and self-care behaviors such as taking meds regularly, keeping a good diet, exercise etc. This inability to carry out self care lifestyle changes may be due to a condition called apathy. Apathy is a lack of motivation and persistence. In this study we will attempt to treat apathy with a medication called methylphenidate for 6 months and see if blood sugar/diabetes control improves.

NCT ID: NCT00767091 Completed - Parkinson's Disease Clinical Trials

Study of Rivastigmine to Treat Parkinsonian Apathy Without Dementia

CHoPA-I
Start date: March 2009
Phase: Phase 3
Study type: Interventional

Apathy usually refers to a set of behavioural, emotional and cognitive features as a reduced interest and participation in main activities of daily life, a lack of initiative, a trend toward an early withdrawal from started activities, an indifference and a flattening of affect. We have validated a new specific scale (Lille Apathy Rating Scale, LARS) in order to detect and quantify apathy in Parkinson's disease (PD). Apathy was shown to be frequent in PD with a prevalence of 32%. It has suggested that the medial frontal and limbic cholinergic deficits may underlie apathy in neurodegenerative disorders like Alzheimer's disease (AD). Such a hypothesis is supported by recent evidence indicating the beneficial effects of cholinesterase inhibitors on neuropsychiatric symptoms, mainly apathy, in AD patients. As the efficacy of rivastigmine on cognition has also been shown in PD, we aimed to assess with a randomized, double-blind, placebo-controlled, parallel-group, multicenter trial, the efficacy and acceptability of a 6 months treatment with rivastigmine on apathy in 60 patients with PD without dementia. The primary end point will be the LARS score and the secondary end points will be the cognitive, behavioural and motor symptoms of PD. Two add-on studies will be proposed: first the measure of choline and glutamate peaks on Magnetic Resonance Spectrometry focused on the structures implicated in apathy in order to give insights in the physiopathological mechanisms of the treatment. Secondly, the recording of the REM sleep behavior disorders in relation with the cholinergic part of the pedunculopontine nucleus. Regarding that apathy could be one of the first steps toward PD dementia, treating very early could have substantial implications on the patients and their caregiver.

NCT ID: NCT00548652 Completed - Obesity Clinical Trials

Role of Apathy in the Effectiveness of Weight Loss Interventions

Start date: August 2007
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether treating apathy with methylphenidate or medical Crisis counselling will increase adherence to weight loss programs thereby increasing their effectiveness

NCT ID: NCT00495820 Completed - Dementia Clinical Trials

Methylphenidate for Apathy in Alzheimer's Dementia: A Controlled Study

Start date: August 2007
Phase: Phase 4
Study type: Interventional

The purpose of the study is to determine the efficacy of methylphenidate over placebo in treating apathy in patients with Alzheimer's dementia. Apathy is one of the earliest and most profound disturbances that occur in Alzheimer's dementia (AD). Hypotheses: 1. Methylphenidate (MPH) will improve apathy significantly more than placebo in AD. 2. Successful treatment of apathy will improve Instrumental Activities of Daily Living (IADLs), and caregiver burden.

NCT ID: NCT00456820 Completed - Depression Clinical Trials

Wellbutrin XL Effects on SSRIs Induced Changes

Start date: July 2004
Phase: Phase 4
Study type: Interventional

The purpose of this study is to find out differences in activation of mood regulating areas of the brain in response to negative and positive pictures, before and after 6 weeks of additional Wellbutrin XL treatment. Participants should have been treated for depression with an SSRI medication (e.g., Prozac, Zoloft, Paxil, Celexa or Lexapro) and have decreased depression symptoms but also be experiencing side effects of medications such as sexual side effects and feelings of apathy (indifference, lack of interest) and lack of full emotional response. We will first take a brain scan to measure activity in different parts of the brain, while subjects are seeing pictures, using Magnetic Resonance Imaging (MRI) scan. Then we will add Wellbutrin XL - another well-known antidepressant that acts by increasing the chemical dopamine in the brain, to subjects' treatment. Wellbutrin addition is useful in decreasing the sexual side effects of SSRIs. After treatment with Wellbutrin XL for 6 weeks subjects will have a second MRI scan with picture rating.