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Effects of a Pedometer-based Unsupervised Exercise Program Upon Lifestyle Physical Activity of Asthmatic Adults

Effects of a Pedometer-based Unsupervised Exercise Program Upon Lifestyle Physical Activity of Asthmatic Adults

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01984281
Enrollment
37
Registered
2013-11-14
Start date
2013-11-30
Completion date
2015-12-31
Last updated
2017-02-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Asthma

Keywords

Physical Activity, Pedometers, Quality of Life

Brief summary

The purpose of this study is to determine whether a pedometer-based unsupervised exercise program is more effective than a general exercise recommendation to increase lifestyle physical activity in adult patients with asthma.

Detailed description

The patients will be randomized in two groups: the intervention group will receive a standardized advice to physical activity practice plus pedometers and step goals to achieve over the next twelve weeks and the control group will receive the same standardized advice to physical activity practice and usual care.

Interventions

BEHAVIORALPedometer-based physical activity prescription

After baseline assessments, both groups will receive a educational session, regarding important aspects of asthma plus a unsupervised exercise prescription (walking, 5 times per week, for at least 30 minutes). Only the experimental group will receive a pedometer-based physical activity prescription, consisting of targets (steps per day) to be achieved. The initial target will be determined based on the average of steps per day assessed during the baseline assessments plus 1000 steps. The targets will be biweekly. Both groups will be contact once a week (by phone) and will be asked to return for asthma control assessments once a month.

Sponsors

Federal University of Juiz de Fora
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Asthma diagnosis for at least 6 months (according to Global Initiative for Asthma criteria) * Regular drug therapy (inhaled corticosteroids or inhaled corticosteroids plus long-acting beta-agonists) * Clinical stability during the run-in period (3 weeks)

Exclusion criteria

* Physical activity practice over once a week * Disabling musculoskeletal disease * Cardiopathy * Other lung disease * More than 10 pack-years of smoking * Pregnancy * Refusal to participate

Design outcomes

Primary

MeasureTime frameDescription
Lifestyle physical activity12 weeksThe lifestyle physical activity will be estimated as the mean number of steps taken in six days using a pedometer (SW200, YAMAX,Tokyo, Japan)

Secondary

MeasureTime frameDescription
Exercise capacity12 weeksExercise capacity will be assessed through the six-minute walking teste.
Asthma Health related quality of life12 weeksAsthma Health related quality of life will be assessed through the Asthma Quality of Life Questionnaire.
Asthma Control12 weeksAsthma Control will be assessed through the Asthma Control Questionnaire
Depression and anxiety12 weeksDepression and anxiety will be assessed through the Hospital Anxiety and Depression Scale
Asthma exacerbations12 weeksAsthma exacerbations will be assessed through exacerbation diaries.

Countries

Brazil

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026