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Completed

NCT Number: NCT02911402

Motion Sickness on Astrolabe's Vessel

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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Key information

Age range

18 year–70 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Caen University Hospital

Caen, 14033, France

About this study

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.).

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • participant aged of 18 or older but younger than 70 who received their medical ability to travel to Terre Adélie or making a research cruise aboard the Astrolabe
  • particpant signing the informed consent.

Exclusion criteria

  • none

Treatment and study plan

sea sickness questionnaires

Other

Primary outcomes

  1. Motion Sickness susceptibilty questionnaire (fMSSQ)

    Time frame: day 1 to day 10

    Sensitivity of motion sickness

  2. STAY-YA questionnaire

    Time frame: day 1 to day 10

    anxiety

  3. STAY-YB questionnaire

    Time frame: day 1 to day 10

    anxiety

  4. Vis-Morgen Questonnaire about sleeping

    Time frame: day 1 to day 10

    Subjective sleep scoring

  5. Fatigue questionnaire

    Time frame: day 1 to day 10

    Tiredness

  6. Dietary intake survey

    Time frame: day 1 to day 10

    food intake

Secondary outcomes

  1. type of movement from the ship using use the data from the Dynamic Positioning System on board

    Time frame: baseline and every day up to 10 days

    boat motion

  2. data from individual actigraphs worn by the participants

    Time frame: baseline and every day up to 10 days

    this will allow to quantify particpant's movements related to the ship movement

  3. personnality questionnaire (OCEAN)

    Time frame: baseline and every day up to 10 days

    Personnality

  4. anxiety questionnaire (STAY).

    Time frame: baseline and every day up to 10 days

    anxiety

  5. treatment taken (international denomination and dose)

    Time frame: baseline and every day up to 6 days

    treatment taken by subject for motion sickness

Sponsors and collaborators

Lead sponsor

University Hospital, Caen

Other

Registry information

Official study title

Evaluation and Characterization of Motion Sickness on Passengers Sailing on the Astrolabe

Acronym: SICKVEST

Important dates

Study start
2014
Primary completion
2017
Study completion
2018
First posted
Sep 22, 2016
Registry last updated
Feb 15, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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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