Effects of Ashtanga-Vinyasa Yoga Supta on Portuguese Airforce Military Pilots Performance

April 17, 2023 updated by: Sara Alexandra Goncalves Santos, University of Évora
A total of 18 military pilots in their tirocinium in the air force academy from the Portuguese Air Force course "Masters in Military Aeronautics: aviator pilot specialist" participated in this study. Participants were randomly assigned to yoga (intervention group) or waiting list (control group). Procedures were approved by the Évora University research ethics committee and participants will give written informed consent according to the Helsinki declaration (approval number: 21050).

Study Overview

Status

Active, not recruiting

Intervention / Treatment

Detailed Description

A randomized, prospective, controlled trial was designed, with the participants (n=18) randomly distributed into two groups. The Control Group (n=8) will be receiving the protocolized classes from the course "Masters in Military Aeronautics: aviator pilot specialist" for 12 weeks, the Intervention Group (n=10) will receive the same course and 2 sessions per week (1h each) of the yoga classes (4). The intensity of the program (Borg rating of perceived exertion scale) will be measured. The operative performance response measurements will be collected at baseline and post-intervention. Participants will complete the following emergency protocols in a flight simulator: (1) take-off engine failure, (2) flight engine failure close to the base, (3) flight engine failure far away from the base, and (4) alternator failure. This intervention protocol was accepted by the Portuguese Airforce to be applied on Airbase 11 in Beja.

Study Type

Interventional

Enrollment (Actual)

18

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Évora, Portugal, 7000-849
        • UEvora

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • healthy military pilots in their tirocinium in the air force academy from the Portuguese Air Force course "Masters in Military Aeronautics: aviator pilot specialist

Exclusion Criteria:

  • military pilots on active duty before or after the tirocinium;
  • injured military pilots;
  • military pilots on sudden lifestyle changes (as in: starting or quitting smoking habits; starting or quitting any kind of medication; starting a new diet)

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Other
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Yoga
Yoga practice: 12-week program of Ashtanga Vinyasa Yoga Supta for 1h twice a week
Ashtanga (asta - eight, anga - parts); Vinyasa (freely sequenced practice); Yoga (practice for evolution); Supta (closed eyes)
Other Names:
  • Yoga class
No Intervention: Waiting list
Only mandatory pilot trainig that everyone in the academy receives

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Changes in Operative performance
Time Frame: measured at 12 weeks (versus baseline values)
Flight times to complete tasks in the flight simulator and report from the flight simulator controler
measured at 12 weeks (versus baseline values)
Changes in Stress and HRV
Time Frame: measured at 12 weeks (versus baseline values)
Heart rate variability measured with Polar H10 portable device
measured at 12 weeks (versus baseline values)
Changes in Vestibular system control responses
Time Frame: measured at 12 weeks (versus baseline values)
Postural control responses through CoP displacement measured with a portable force platform Biosignals Plux with data sampled at 1000 Hz and electrode impedance below 5 kΩ. Preprocessing performed using the EEGLAB toolbox, which is available for use in MATLAB (The MathWorks Inc., Natick, MA). Data downsampled to 100 Hz.
measured at 12 weeks (versus baseline values)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Changes in Body composition
Time Frame: measured at 12 weeks (versus baseline values)

Body composition data (percent body fat, percent fat free mass, percent muscle mass index, as a percentages) measured with a Tanita (MC-780 MA, Tanita, Tokyo, Japan) to get a bioelectrical impedance analysis (BIA) will indicate if the exercise protocol had any impact in the pilot's physical makeup.

Percent body fat, percent fat-free mass, and percent muscle mass index are all related to body composition. Here's how they relate to each other: Percent body fat is the percentage of body weight that is made up of fat and includes both essential and storage fat; Percent fat-free mass is the percentage of body weight that is not fat and includes muscle, bone, organs, and other non-fat tissues; Percent muscle mass index is the percentage of body weight that is muscle. Percent body fat and percent fat-free mass are complementary measures that add up to 100%, while percent muscle mass index is a measure of the proportion of muscle in the body weight.

measured at 12 weeks (versus baseline values)
Changes in Lung capacity
Time Frame: measured at 12 weeks (versus baseline values)
Ventilatory response measured with spirometry - FEV1/FVC ratio indicates how much air you can forcefully exhale
measured at 12 weeks (versus baseline values)
Five Facet Mindfulness Questionnaire - Changes in cognitive habilities
Time Frame: measured at 12 weeks (versus baseline values)
FFMQ with 15 questions and average scores are calculated by summing the responses and dividing by the number of items, and indicate the average level of agreement with the each subscale (1 = rarely true, 5 = always true). Higher scores are indicative of someone who is more mindful in their everyday life.
measured at 12 weeks (versus baseline values)
Multidimensional Assessment of Interoceptive Awareness Questionnaire - Changes in cognitive habilities
Time Frame: measured at 12 weeks (versus baseline values)
MAIA - is an 8-scale state-trait questionnaire with 32 items to measure multiple dimensions of interoception; scores are between 0 and 5, where higher score equates to more awareness of bodily sensation.
measured at 12 weeks (versus baseline values)
Aviation Safety Attitude Scale - Changes in cognitive habilities
Time Frame: measured at 12 weeks (versus baseline values)
ASAS - consists of. 27 items on a five-point scale, each designed specifically to assess pilots' attitudes with respect to predict the hazardous event involvement of aviators; For all the attitude subscales, higher scores indicate a greater degree of that particular attitude - For example, higher scores on the ASAS self-confidence factor indicated that the person expressed greater confidence in their ability as a pilot
measured at 12 weeks (versus baseline values)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Sara G Santos, University of Évora

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

March 1, 2021

Primary Completion (Actual)

September 1, 2022

Study Completion (Anticipated)

September 1, 2023

Study Registration Dates

First Submitted

February 8, 2023

First Submitted That Met QC Criteria

April 17, 2023

First Posted (Actual)

April 20, 2023

Study Record Updates

Last Update Posted (Actual)

April 20, 2023

Last Update Submitted That Met QC Criteria

April 17, 2023

Last Verified

April 1, 2023

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • UEvora approval number: 21050

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

IPD that underlie results in a publication

IPD Sharing Time Frame

2023 onwards

IPD Sharing Access Criteria

Depends on the Journal that publishes the data

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL
  • SAP
  • ICF

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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