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Influence of Music on 6 Minutes Walking Distance in Healthy Children

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ClinicalTrials.gov Identifier: NCT01829438
Recruitment Status : Completed
First Posted : April 11, 2013
Last Update Posted : April 11, 2013
Sponsor:
Information provided by (Responsible Party):
G.Reychler, Cliniques universitaires Saint-Luc- Université Catholique de Louvain

Brief Summary:
To evaluate the effect of different distractive auditory stimuli (fast, slow and preferred) on 6 Minute Walking Test (6MWT) and the measured parameters (dyspnea, heart rate, oxygen saturation) in healthy children.

Condition or disease Intervention/treatment Phase
Healthy Children Behavioral: Listening to fast music Behavioral: Listening to preferred music Behavioral: Listening to slow music Not Applicable

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 97 participants
Allocation: Randomized
Intervention Model: Crossover Assignment
Masking: Single (Outcomes Assessor)
Primary Purpose: Supportive Care
Official Title: Influence of a Distractive Auditory Stimulus on 6 Minute Walking Test in Healthy Children
Study Start Date : June 2010
Actual Primary Completion Date : June 2010
Actual Study Completion Date : June 2011

Arm Intervention/treatment
No Intervention: Without music
6MWT without music
Experimental: With fast music
6MWT with a fast music
Behavioral: Listening to fast music
Other Name: Listening to fast music during the test

Experimental: With slow music
6MWT with a slow music
Behavioral: Listening to slow music
Other Name: Listening to preferred music during the 6MWT

Experimental: With preferred music
6MWT with the preferred music of the child
Behavioral: Listening to preferred music
Other Name: Listening to preferred music during the 6MWT




Primary Outcome Measures :
  1. Walked distance [ Time Frame: After 6 minutes ]
    The distance walked by subjects during a 6 minutes walking test


Secondary Outcome Measures :
  1. Dyspnea [ Time Frame: At the end of the 6MWT ]
    Dyspnea is measured by a visual analogue scale


Other Outcome Measures:
  1. cardio-respiratory parameters [ Time Frame: at the begining and the end of the 6MWT ]
    Heart rate and oxygen saturation are measured before and after the test



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Ages Eligible for Study:   5 Years to 18 Years   (Child, Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • the participation to the physical education program after the annual medical investigation

Exclusion Criteria:

  • a lung disease
  • an overweight
  • a motor disability based on parent's answers to a questionnaire

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01829438


Locations
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Belgium
UCL
Brussels, Belgium, 1200
Sponsors and Collaborators
Cliniques universitaires Saint-Luc- Université Catholique de Louvain
Investigators
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Principal Investigator: Lux Amandine, Student UCL
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Responsible Party: G.Reychler, Doctor in Physiotherapy, Cliniques universitaires Saint-Luc- Université Catholique de Louvain
ClinicalTrials.gov Identifier: NCT01829438    
Other Study ID Numbers: 6MWT
First Posted: April 11, 2013    Key Record Dates
Last Update Posted: April 11, 2013
Last Verified: April 2013
Keywords provided by G.Reychler, Cliniques universitaires Saint-Luc- Université Catholique de Louvain:
exercise tolerance
6MWT