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Clinical Trials/TCTR20170209001
TCTR20170209001
Recruiting
未知

The Effects of High Intensity Interval Training Combined with Resistance Training on Sleep Breathing Variables and Vascular Function in Children and Adolescents with Obstructive Sleep Apnea Syndrome

Graduate student of Chiang Mai University0 sites42 target enrollmentFebruary 9, 2017

Overview

Phase
未知
Intervention
Not specified
Conditions
Obese children and adolescents with obstructive sleep apnea syndrome
Sponsor
Graduate student of Chiang Mai University
Enrollment
42
Status
Recruiting
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
February 9, 2017
End Date
December 1, 2017
Last Updated
last year
Study Type
Interventional
Sex
All

Investigators

Sponsor
Graduate student of Chiang Mai University

Eligibility Criteria

Inclusion Criteria

  • 1\.Boy or girl aged 7\-18 years old who have confirmed of OSAS (AHI \> 1 or ODI \> 1 or SaO2nadir \< 92%) by using an overnight polosomnography (PSG) (3, 11\).
  • 2\.Subjects who defined as overweight or obese individual, according to the criteria of the International Obesity Task Force (IOTF) (61\).

Exclusion Criteria

  • 1\) Subjects who had received other treatments that would influence study results e.g. CPAP therapy, medicines involved in weight control, behavioral modification and the other exercise program
  • 2\) Subjects who had any existing contraindications for exercise testing according to ACSM’s guideline
  • 3\) Subjects who had medical conditions that would affect study results i.e., symptomatic cardiac disease, hypertension (HT), diabetes mellitus (DM), any neurological deficits (i.e., dementia and poor mental status) and orthopedic problems that limit ability to ambulation or walking and
  • 4\) Subjects who had any implanted metal accessories.
  • In addition, participant’s data would not be summarized if they demonstrate any of the following criteria;
  • 1\) Participants who had exercise adherence rate lesser than 85 percent of total exercise session (20/24 sessions)
  • 2\) Participants who were not willing to continue the program of the study.

Outcomes

Primary Outcomes

Not specified

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