Caen University Hospital
Caen, 14033, France
NCT Number: NCT02911402
Sea sickness syndrome is present for 80% of persons on board when the boat rotation missions Astrolabe, sometimes there is a risk of very significant dehydration. A special unit specialized in the fundamental study of the vestibular system (inner ear), sensory organ at the base of visual-vestibular conflict inducing this syndrome, also provides medical support for parabolic flights (flight reproducing weightlessness) where this syndrome is strongly present. The goal of the study is to assess the frequency of occurrence of this sea sickness syndrome on the Astrolabe, to understand the triggers (type of boat movements, personality traits, anxiety / stress) without changing habits on board for those on board taking a antinaupathique treatment given by the ship's doctor. This study will be done in collaboration between INSERM U 1075 (France) and the Laboratory of military research VIPER specialized in extreme environments (Belgium). The ultimate goal will be to provide the best recommendations and the best treatment regimen to alleviate as best as possible the symptoms of people on board of the Astrolabe so scientists on board can perform their work.
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Notify Me18 year–70 year
All sexes
Observational
Caen, 14033, France
Background: The objectives were to assess the prevalence, severity, medication taken and to look for predictive factors, in order to better identify characteristics of passengers at risk of motion sickness during transport scientists travelling from Hobart in Tasmania to the French polar stations in Antarctica.
Methods: Two hundred and thirty-nine passengers were surveyed over 4 years with 4 round trips per year using Motion Sickness Susceptibility Questionnaire (MSSQ), Simulator Sickness Questionnaire (SSQ), state-trait anxiety test (STAI-Trait and STAI-State), and general parameters (age, gender, number of trips, jet-lag, direction of the trip), medication, calculation of the distance of each passenger's cabin to the Centre of Gravity (CoG.).
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: day 1 to day 10
Sensitivity of motion sickness
Time frame: day 1 to day 10
anxiety
Time frame: day 1 to day 10
anxiety
Time frame: day 1 to day 10
Subjective sleep scoring
Time frame: day 1 to day 10
Tiredness
Time frame: day 1 to day 10
food intake
Time frame: baseline and every day up to 10 days
boat motion
Time frame: baseline and every day up to 10 days
this will allow to quantify particpant's movements related to the ship movement
Time frame: baseline and every day up to 10 days
Personnality
Time frame: baseline and every day up to 10 days
anxiety
Time frame: baseline and every day up to 6 days
treatment taken by subject for motion sickness
University Hospital, Caen
Other
Evaluation and Characterization of Motion Sickness on Passengers Sailing on the Astrolabe
Acronym: SICKVEST
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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