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Exploring the Use of Transdermal Methylphenidate to Reduce Fall Risk in Patients With Dementia.

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Ce qui est testé

Transdermal Methylphenidate

Médicament
Qui peut participer

Troubles Mentaux+11

+ Maladies du cerveau

+ Maladies du système nerveux central

De 65 à 95 ans
Voir tous les critères d'éligibilité
Comment se déroule l'étude

Étude de prévention

Phase 4
Interventionnel
Date de début : novembre 2012
Voir le détail du protocole

Résumé

Sponsor principalSt. Louis University
Dernière mise à jour : 24 juillet 2018
Issu d'une base de données validée par les autorités. Revendiquer en tant que partenaire

Date de début de l'étude : 1 novembre 2012

Date à laquelle le premier participant a commencé l'étude.

This is an open label pilot study; consenting subjects with dementia and identified as a fall risk, who meet inclusion criteria will undergo 3 phases of involvement. Phase 1 is a 1 week period before initiating study drug. Phase 2 is a 2 week treatment period with 10mg of Transdermal Methylphenidate. Phase 3 is the final two week treatment period with 15mg of Transdermal Methylphenidate. Measurements obtained at each phase will include: Vital Signs (blood pressure and pulse rate) weight , Timed Get Up and Go Test (TUG) , Tinetti Performance Oriented Mobility Assessment (POMA), Clinical Apathy Evaluation Scale (AES-C) and the St. Louis University Mental Status Examination (SLUMS). The primary endpoint is the change in TUG and POMA scores at end of phase 3 compared to beginning of phase 2 Falls are a cause of substantial morbidity and mortality in patients with dementia and occur at twice the rate of older adults without cognitive impairment. The consequences of falls in older adults with dementia are serious; fallers with cognitive problems are approximately five times as likely to be admitted to institutional care as people with cognitive problems who do not fall.[3] They are also at high risk of major fall-related injuries such as fractures and head injuries that increase mortality risk. Walking requires paying attention to various environmental features and recovering from postural variations to avoid stumbles or falls. Consequently, deficits in attention and executive function are independently associated with risk of postural instability, impairment in activities of daily living, and fall risk. Executive function refers to higher cognitive processes that allocate attention among tasks and a critical cognitive resource for normal walking. Lower scores on executive function measures are associated with both dementia and a higher fall risk. Although significant progress towards understanding the factors involved in falls has been made, the number of falls and fall related injuries continue to increase. Changes in aging demographics are expected to dramatically increase the aging population and dementia prevalence, underscoring the importance of developing more effective fall prevention strategies. Recent studies have shown that improving certain aspects of cognition, specifically attention and executive function, in older adults can improve mobility decline and risk of falls. Particularly in cognitively impaired individuals, this may be critical to reducing fall risk. Why Methylphenidate? Pharmacological properties of psychostimulants, such as methylphenidate (MPH), are known to increase executive function. Methylphenidate was chosen because of the studies demonstrating the safe use of MPH for treatment of depression and apathy in the cognitively impaired elderly and the well-studied effects of MPH on executive function and attention in children and adults with ADHD. Also a small study published in April 2008 in J Am Geriatric Society, evaluated the use of methylphenidate in reducing fall risk among community living older adults. The study concluded that among study subjects receiving methylphenidate, significant improvement in mobility and gait assessments were observed as well as drug tolerability. The basis for our study is to further explore the pharmacotherapeutic role of Transdermal-MPH in reducing fall risk in dementia patients. Mobility and gait assessment performance is strongly correlated with fall risk. Therefore we will use subject's scores before, during and after medication administration to measure response and evaluate use as a fall prevention strategy.

Sponsor principalSt. Louis University
Dernière mise à jour : 24 juillet 2018
Issu d'une base de données validée par les autorités. Revendiquer en tant que partenaire

Protocole

Cette section fournit des détails sur le plan de l'étude, y compris la manière dont l'étude est conçue et ce qu'elle évalue.
Détails du design

14 participants à inclure

Nombre total de participants que l'essai clinique vise à recruter.

Prévention

Cette étude cherche à prévenir l'apparition d'une maladie ou d'un trouble chez des personnes qui ne l'ont pas encore développé. Elles concernent souvent des personnes à risque et testent des vaccins, des changements de mode de vie ou des traitements préventifs.



Éligibilité

Les chercheurs recherchent des patients correspondant à une certaine description appelée critères d'éligibilité : état de santé général ou traitements antérieurs du patient.
Conditions
Critères

Tout sexe

Le sexe biologique des participants éligibles à s'inscrire.

De 65 à 95 ans

Tranche d'âge des participants éligibles à participer.

Volontaires sains non autorisés

Indique si les individus en bonne santé et ne présentant pas la condition étudiée peuvent participer.

Conditions

Pathologie

Troubles MentauxMaladies du cerveauMaladies du système nerveux centralMaladies du système nerveuxManifestations NeurologiquesSignes et symptômesConditions pathologiques, signes et symptômesMaladies neurodégénérativesManifestations NeurocomportementalesTroubles NeurocognitifsTauopathiesMaladie d'AlzheimerDémenceLéthargie

Critères

Inclusion Criteria: 65- 95 years of age Ability to ambulate (may use walking aid) Male or Female Clinical diagnosis of Dementia Identified as fall risk by nursing staff Exclusion Criteria: Clinically significant musculoskeletal, cardiovascular or respiratory diseases. Clinically significant vestibular disorder History of significant head trauma Any medically unstable condition, as determined by the PI that would expose patient to potential harm. Patients taking medications that may interact with MPH, as determined by manufacture's package insert. Including but not limited to: Warfarin, anticonvulsants, MAOIs, alpha2-agonists, tri-cyclic antidepressants. Legally Blind History of seizures, Poorly controlled hypertension, cardiac arrhythmia or cardiovascular disease, heart failure. Known or suspected allergy to MPH or similar compounds Glaucoma Motor tics History of significant agitation or anxiety Family history of Tourette's syndrome History of significant anxiety History of significant agitation History of significant tension.

Plan de l'étude

Découvrez tous les traitements administrés dans cette étude, leur description détaillée et ce qu'ils impliquent.
Groupes de traitement
Objectifs de l'étude

Un seul groupe d'intervention est désigné dans cette étude

Cette étude ne comporte pas de groupe placebo. 

Groupes de traitement

Groupe I

Expérimental
2 Weeks of once daily 10mg Transdermal Methylphenidate followed by 2 weeks of once daily 15mg Transdermal Methylphenidate. Patch will be worn for approximately 7-10hrs each day.

Objectifs de l'étude

Objectifs principaux

Objectifs secondaires

Centres d'étude

Ce sont les hôpitaux, cliniques ou centres de recherche où l'essai est conduit. Vous pouvez trouver le site le plus proche de vous ainsi que son statut.

Cette étude comporte 1 site

Delmar Gardens

St Louis, United StatesOuvrir Delmar Gardens dans Google Maps
Suspendu1 Centres d'Étude