Effects of Allergic Rhinitis on Cognition and Driving (upu055)

The recruitment status of this study is unknown because the information has not been verified recently.
Verified November 2010 by Maastricht University Medical Center.
Recruitment status was  Not yet recruiting
Sponsor:
Information provided by:
Maastricht University Medical Center
ClinicalTrials.gov Identifier:
NCT01239264
First received: November 10, 2010
Last updated: NA
Last verified: November 2010
History: No changes posted
  Purpose

Previous research has shown that patients suffering from Allergic Rhinitis (AR) not only suffer from direct symptoms of their condition but also report a decreased quality of life. More specific this relates not only to psychological wellbeing but also to diminished cognitive functions such as memory and concentration. In a recent study of a group the investigators showed that in tasks with a higher and longer lasting cognitive load symptomatic AR patient performed significantly worse compared to controls. The finding of a direct relationship between AR symptoms and cognitive functioning strongly suggests implications of AR daily life functioning, safety and workplace productivity. Whereas untreated AR was previously thought only to affect subjective wellbeing it now seems that cognitive functioning might be directly impaired which could lead to potentially dangerous situations in daily life such as driving a car or operating machinery. In this study the investigators will research the effect of an allergen challenge in AR patients on actual driving and memory functions. A comparison in performance will be made between untreated patients and patients treated with systemic or topical drugs.


Condition Intervention Phase
Seasonal Allergic Rhinitis
Drug: cetirizine 10mg and Fluticasone Furoate
Phase 4

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Pharmacodynamics Study
Intervention Model: Crossover Assignment
Masking: Double Blind (Subject, Investigator, Outcomes Assessor)
Official Title: Effects of Treated and Untreated Allergic Rhinitis on Mood, Cognitive Functions and Actual Driving Performance

Resource links provided by NLM:


Further study details as provided by Maastricht University Medical Center:

Primary Outcome Measures:
  • Standard Deviation of Lateral Position (SDLP) [ Time Frame: 90 - 150 minutes post challenge ] [ Designated as safety issue: No ]
    Primary measure is performance in an over the road driving test as measured by the ability to keep within the boundaries of the slower traffic of a highway during a 60 minute driving test


Secondary Outcome Measures:
  • WLT 15 memory test score [ Time Frame: 120 minutes post challenge ] [ Designated as safety issue: No ]
    The secondary outcome score is the total number of words correctly remembered on a 15-word learning test administered during the driving test


Estimated Enrollment: 20
Study Start Date: November 2010
Estimated Study Completion Date: June 2011
Estimated Primary Completion Date: May 2011 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Placebo Comparator: Placebo drug + placebo pollen challenge
Placebo treatment after placebo (sham) nasal pollen challenge
Drug: cetirizine 10mg and Fluticasone Furoate
Subjects will undergo a nasal pollen challenge or sham challenge followed by treatment with either a systemic, topical or placebo treatment.
Active Comparator: placebo drug + active pollen challenge
A placebo treatment with active pollen nasal challenge
Drug: cetirizine 10mg and Fluticasone Furoate
Subjects will undergo a nasal pollen challenge or sham challenge followed by treatment with either a systemic, topical or placebo treatment.
Experimental: Systemic drug + active pollen treatment Drug: cetirizine 10mg and Fluticasone Furoate
Subjects will undergo a nasal pollen challenge or sham challenge followed by treatment with either a systemic, topical or placebo treatment.
Experimental: topical drug + active pollen challenge Drug: cetirizine 10mg and Fluticasone Furoate
Subjects will undergo a nasal pollen challenge or sham challenge followed by treatment with either a systemic, topical or placebo treatment.

  Eligibility

Ages Eligible for Study:   20 Years to 40 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Diagnosed as SAR patient
  • Experienced driver

Exclusion Criteria:

  • History of neurological or psychiatric disease
  • use of psychoactive medication
  • clinical abnormalities at medical screening
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01239264

Locations
Netherlands
Maastricht University Not yet recruiting
Maastricht, Limburg, Netherlands, 6200MD
Contact: Eric Vuurman, PhD     +31433881046     eric.vuurman@maastrichtuniversity.nl    
Principal Investigator: Eric Vuurman, PhD            
Sponsors and Collaborators
Maastricht University Medical Center
  More Information

Publications:
Responsible Party: Dr. Eric Vuurman, Maastricht University
ClinicalTrials.gov Identifier: NCT01239264     History of Changes
Other Study ID Numbers: 10.1.044
Study First Received: November 10, 2010
Last Updated: November 10, 2010
Health Authority: The Netherlands: The central committee on research involving human subjects (CCMO)

Keywords provided by Maastricht University Medical Center:
Seasonal Allergic Rhinitis
Driving performance
memory
mood

Additional relevant MeSH terms:
Rhinitis, Allergic, Seasonal
Rhinitis
Nose Diseases
Respiratory Tract Diseases
Respiratory Hypersensitivity
Otorhinolaryngologic Diseases
Hypersensitivity, Immediate
Hypersensitivity
Immune System Diseases
Respiratory Tract Infections
Fluticasone
Cetirizine
Anti-Allergic Agents
Therapeutic Uses
Pharmacologic Actions
Histamine H1 Antagonists, Non-Sedating
Histamine H1 Antagonists
Histamine Antagonists
Histamine Agents
Neurotransmitter Agents
Molecular Mechanisms of Pharmacological Action
Physiological Effects of Drugs
Bronchodilator Agents
Autonomic Agents
Peripheral Nervous System Agents
Anti-Asthmatic Agents
Respiratory System Agents
Dermatologic Agents
Anti-Inflammatory Agents

ClinicalTrials.gov processed this record on May 16, 2013