Working…
COVID-19 is an emerging, rapidly evolving situation.
Get the latest public health information from CDC: https://www.coronavirus.gov.

Get the latest research information from NIH: https://www.nih.gov/coronavirus.
ClinicalTrials.gov
ClinicalTrials.gov Menu

Influence of Music on 6 Minutes Walking Distance in Healthy Children

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
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

Study Description
Go to 
Top of Page Study Description Study Design Arms and Interventions Outcome Measures Eligibility Criteria Contacts and Locations More Information
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

Study Design
Go to 
Top of Page Study Description Study Design Arms and Interventions Outcome Measures Eligibility Criteria Contacts and Locations More Information

Layout table for study information
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
Arms and Interventions
Go to 
Top of Page Study Description Study Design Arms and Interventions Outcome Measures Eligibility Criteria Contacts and Locations More Information

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


Outcome Measures
Go to 
Top of Page Study Description Study Design Arms and Interventions Outcome Measures Eligibility Criteria Contacts and Locations More Information

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


Eligibility Criteria
Go to 
Top of Page Study Description Study Design Arms and Interventions Outcome Measures Eligibility Criteria Contacts and Locations More Information

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Layout table for eligibility information
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
Contacts and Locations
Go to 
Top of Page Study Description Study Design Arms and Interventions Outcome Measures Eligibility Criteria Contacts and Locations More Information

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
Layout table for location information
Belgium
UCL
Brussels, Belgium, 1200
Sponsors and Collaborators
Cliniques universitaires Saint-Luc- Université Catholique de Louvain
Investigators
Layout table for investigator information
Principal Investigator: Lux Amandine, Student UCL
More Information
Go to 
Top of Page Study Description Study Design Arms and Interventions Outcome Measures Eligibility Criteria Contacts and Locations More Information
Layout table for additonal information
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