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Investigating the safety and efficacy of nabilone for the treatment of agitation in patients with moderate-to-severe Alzheimer's disease: Study protocol for a cross-over randomized controlled trial
- Source :
- Contemporary Clinical Trials Communications, Contemporary Clinical Trials Communications, Vol 15, Iss, Pp-(2019)
- Publication Year :
- 2019
- Publisher :
- Elsevier, 2019.
-
Abstract
- Agitation is a prevalent and difficult-to-treat symptom in patients with moderate-to-severe Alzheimer's disease (AD). Though there are nonpharmacological and pharmacological interventions recommended for the treatment of agitation, the efficacy of these are modest and not always consistent. Furthermore, the safety profiles of currently prescribed medications are questionable. Nabilone, a synthetic cannabinoid, has a distinct pharmacological profile that may provide a safer and more effective treatment for agitation, while potentially having benefits for weight and pain. Additionally, emerging evidence suggests nabilone may have neuroprotective effects. We describe a clinical trial investigating the safety and efficacy of nabilone for the treatment of agitation in patients with moderate-to-severe AD. This will be a double-blind, randomized cross-over study comparing 6 weeks of nabilone (0.5–2 mg) and placebo, with a 1-week washout preceding each phase. Study outcomes will be measured at baseline and end of treatment for each treatment phase. The primary outcome measure will be agitation as assessed by the Cohen-Mansfield Agitation Inventory. The secondary outcomes include safety, behaviour (Neuropsychiatric Inventory), cognition (standardized Mini Mental Status Exam and either Severe Impairment Battery or Alzheimer's disease Assessment Scale-Cognitive subscale) and global impression (Clinician's Global Impression of Change). Exploratory outcomes include pain (Pain Assessment in Advanced AD), nutritional status (Mini-Nutritional Assessment-Short Form), caregiver distress (NPI caregiver distress), and blood-based biomarkers. A safe and efficacious pharmacological intervention for agitation, with effects on pain and weight loss in patients with moderate-to-severe AD could increase quality-of-life, reduce caregiver stress and avoid unnecessary institutionalization and related increases in health care costs. Clinical trials number: NCT02351882 Keywords: Agitation, Cannabinoid, Alzheimer's disease, Neuropsychiatric symptoms, Clinical trial
- Subjects :
- LTC, long-term care
THC, tetrahydrocannabinol
Disease
NPI-NH, Neuropsychiatric Inventory-Nursing home version
law.invention
0302 clinical medicine
CGIC, Clinician's Global Impression of Change
Randomized controlled trial
Pain assessment
Weight loss
law
CB2, cannabinoid receptor 2
030212 general & internal medicine
RCT, randomized controlled trial
2. Zero hunger
IPA, International Psychogeriatric Association
lcsh:R5-920
CB, cannabinoids
sMMSE, standardized Mini-Mental Status Examination
CB1, cannabinoid receptor 1
NPS, neuropsychiatric symptoms
General Medicine
Alzheimer's disease
3. Good health
Neuropsychiatric symptoms
Clinical trial
SIB, Severe Impairment Battery
Caregiver stress
EC50, half maximal effective concentration
AD, Alzheimer's disease
medicine.symptom
PAINAD, Pain Assessment in Advanced AD
lcsh:Medicine (General)
medicine.drug
medicine.medical_specialty
Placebo
Article
MNA-SF, Mini-Nutritional Assessment-Short form
03 medical and health sciences
medicine
Cannabinoid
Pharmacology
Agitation
business.industry
medicine.disease
FDA, Food and Drug Administration
Nabilone
Physical therapy
CMAI, Cohen Mansfield Agitation Inventory
MAR, Medication Administration Record
business
030217 neurology & neurosurgery
Subjects
Details
- Language :
- English
- ISSN :
- 24518654
- Volume :
- 15
- Database :
- OpenAIRE
- Journal :
- Contemporary Clinical Trials Communications
- Accession number :
- edsair.doi.dedup.....b1be3165ca8efd218d9878e978fa61f3