CClinicalTrials.gg
Status unknownNCT03653949Updated Oct 4, 2019

Effects of Aerobic Interval Training on Glucose Tolerance in Children and Adolescents With Cystic Fibrosis

An interventional study of Educational intervention and Aerobic exercise in Cystic Fibrosis, sponsored by Universidade Federal do Rio Grande do Norte. Status unknown at 1 site in Brazil. Open to participants aged 6 Years to 18 Years. Per ClinicalTrials.gov, last updated 2019-10-04.

Sponsored by Universidade Federal do Rio Grande do Norte · Not applicable, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Oct 2019), so the status shown — last known as Recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
20
Allocation
Randomized
Ages
6 Years to 18 Years
Sex
All
01

Study summary

The purpose of this study is to investigate the effects of aerobic exercise on glucose tolerance in individuals with cystic fibrosis.

The hypothesis is that performing High Intensity Interval Training glucose tolerance will improve in individuals with cystic fibrosis.

Read the detailed description

This is a controlled, randomized, and single blind trial. The first researcher (P1) will be responsible for the randomization process; the second researcher (P2) will be responsible for the evaluations and reevaluations. This evaluator (P2) will be "blind", meaning that for him it is totally unknown in which group each patient will be insert; and the third researcher (P3), will be responsible for statistical analysis.

Individuals will be recruited at the Child and Adolescent Health Care Unit of the Onofre Lopes University Hospital (HUOL) and in the Department of Physical Therapy of the State University of Paraíba (UEPB), Campina Grande - PB, Brazil. They will be evaluated at the Physical Therapy Department of the Federal University of Rio Grande do Norte (UFRN), Natal - RN, Brazil and in the Department of Physical Therapy of the State University of Paraíba (UEPB), in the city of Campina Grande - PB. A pilot study will be carried out and the sample calculation will be done with the data collected to reach a statistical power of 80% and a level of significance of 0.05%. Allocation in the groups will be performed by P1, randomly in blocks by the volunteer being prepubertal or pubertal. The R Core Team software (2015) will be used for this process.

In this study two groups will be considered: control group (CG) and aerobic exercise group (AEG). The CG will be submitted to educational intervention. The AEG will be submitted to the same educational intervention and to the High Intensity Interval Training.

After the pilot study, the patients will be evaluated to obtain information on severity and exacerbation of the disease, quality of life, metabolic evaluation, anthropometric measures, and lung function. All evaluations will be carried out at the same day period (morning). Researcher two (P2) will be responsible for the evaluation and reassessment procedure of the individuals, hence he will be "blind" meaning that for him it is totally unknown in which group each patient will be or was inserted. Individuals will be instructed to do not perform physical activity in the day before the evaluations. After this step, individuals will be randomly distributed in CG or EAG.

Volunteers from both groups will be instructed to maintain nutritional, drug and secretion care. In addition, they will be instructed to do not get engaged in any other kind of physical activity. The intervention will last 2 months and will occur 3 times a week until a total of 24 sessions. After the intervention ends and after the 8-week follow-up, all volunteers will be reevaluated.

02

Conditions studied

  • Cystic Fibrosis

Keywords

  • Cystic fibrosis
  • Insulin Resistance
  • Aerobic Exercise
  • Child
  • Adolescents
03

In context

Cystic Fibrosis

1,581 studies on the registry are indexed under Cystic Fibrosis; 190 are open to participants now.

This study's planned enrollment of 20 is below the median of 36 across 1,034 interventional studies indexed under Cystic Fibrosis.

Browse Cystic Fibrosis studies →

Lead sponsor

Universidade Federal do Rio Grande do Norte is the lead sponsor of 84 studies on the registry; 13 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
6 Years to 18 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Diagnosis of cystic fibrosis, according to the Brazilian Guidelines for diagnosis and treatment of CF;
  • Prepubertal or pubertal, according to the Tanner scale
  • Both sex.

Exclusion criteria

Exclusion Criteria:

  • Inability to perform the protocol established to the study;
  • To be unable to understand and / or perform procedures.
  • Exacerbation of the clinical picture, defined as modification and / or addition of antibiotic.
  • To be pregnant.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Investigator, Outcomes assessor)
Enrollment
20 participants (estimated)

Study arms

  • Experimental
    High Intensity Interval Training

    The subjects will participate of an educational intervention and a High Intensity Interval Training.

    Other: Educational intervention · Other: Aerobic exercise

  • Active comparator
    Control Group

    The subjects will participate of an educational intervention.

    Other: Educational intervention

Interventions

  • OtherEducational intervention

    It will be an interactive lecture, 60 minutes long. The class will cover physiopathology, complications, treatment and prevention of exacerbations. Audiovisual resources and practical demonstrations of usual care will be used. Individual questions will be answered during the class.

  • OtherAerobic exercise

    The aerobic exercise program will be performed at home, on a cycle ergometer for lower limbs between 24 and 35 minutes: 5 minutes of warm-up, 14 to 25 minutes of high-intensity interval exercise and 5 minutes of cool down.

06

What researchers measure

Primary outcomes

  1. Change in glucose tolerance

    Glucose tolerance will be determined by measuring fasting Insulin, fasting glucose, OGTT for all patients.

    Time frame: Measured at baseline, after 8 and 16 weeks.

Secondary outcomes

  1. Cystic fibrosis Quality of life

    the Quality of Life Questionnaire in Cystic Fibrosis (QFC) was translated and validated into Portuguese in 2006. There are four versions of the questionnaire, according to age group: 6 to 11 years (35 questions), 12 and 13 years (35 questions), 14 years or more (50 questions) and parents of children between 6 and 11 years old (44 questions). For children between 6 and 11 years old the application of the questionnaire will be assisted by special cards that will designate the child's response. The questionnaire addresses the physical, body image, digestive, respiratory, emotional, social, nutrition, treatment, vitality, health, social role and weight domains. The scores of each domain range from zero to 100, considering a good quality of life if score above 50.

    Time frame: Measured at baseline, after 8 and 16 weeks.

  2. Lung Function

    Forced expired volume in one second (FEV1) and forced vital capacity (FVC), FEV1/FVC ratio, forced expiratory flow at 25-75% of the pulmonary volume (FEF25-75).

    Time frame: Measured at baseline, after 8 and 16 weeks.

  3. Functional capacity

    The 3 minute step test

    Time frame: Measured at baseline, after 8 and 16 weeks.

  4. Respiratory muscle strength

    Maximum respiratory pressure

    Time frame: Measured at baseline, after 8 and 16 weeks.

  5. Exacerbations

    Exacerbations of Cystic Fibrosis through the criteria of Fuchs

    Time frame: Measured at baseline, after 8 and 16 weeks.

07

Study locations

1 of 1 sites recruiting
  • Karolinne Souza Monteiro
    Natal, RN 59064-741, Brazil
    Recruiting
08

References and documents

Publications

  • Monteiro KS, Azevedo MP, Jales LM, da Silva FEP, Arrais RF, de Mendonca KMPP. Effects of aerobic interval training on glucose tolerance in children and adolescents with cystic fibrosis: a randomized trial protocol. Trials. 2019 Dec 26;20(1):768. doi: 10.1186/s13063-019-3803-8. PubMed 31878961 ↗

Individual participant data

Plan to share: No

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 4, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03653949
Lead sponsor
Universidade Federal do Rio Grande do Norte
Collaborators
Universidade Estadual da Paraiba
Responsible party
Karla Morganna Pereira Pinto de Mendonça (Federal University of Rio Grande do Norte, Universidade Federal do Rio Grande do Norte) — Principal investigator
First posted
Aug 31, 2018
Start date
Feb 4, 2019
Primary completion
Dec 2019 (estimated)
Completion
Dec 2020 (estimated)
Last update
Oct 4, 2019

Study contacts

Karolinne Monteiro, Master
Contact
karolsm@outlook.com.br
+5584996387722
Thayla Santino, Master
Contact
thaylaamorim@gmail.com
+5583999424386
Karolinne Monteiro, Master
principal investigator · Universidade Federal do Rio Grande do Norte

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Oct 2019. You cannot join it, but the record below documents what was studied.

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