Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
100 participants
INTERVENTIONAL
2012-04-30
2019-12-31
Brief Summary
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Rationale \& Hypothesis: Different breathing exercise regimens currently recommended are not well defined and in certain cases may worsen dyspnea or even trigger an asthma attack. Therefore, it is important to evaluate the overall usefulness of a breathing exercise as a therapeutic intervention of asthma. In this regard, the investigators have designed an easy, few-minute breathing exercise program as a treatment modality for asthma and to evaluate its efficacy in improving associated clinico-immunological symptoms. The investigators hypothesize that the investigators' well-designed breathing/mild physical exercise intervention for obese patients will help alleviate the stress and symptoms of asthma by reducing the chronic low-grade systemic inflammation and thus potentiate the beneficial outcome of medication to render a better control over the disease and to improve the quality of life in obese patients.
Clinical relevance/Significance:
The investigators expect that their exercise module will help reduce inflammation caused by asthma, and thereby relieving symptoms of asthma. If successful, this would allow regular individualized exercise module to be recommended as a part of therapy for people with asthma, which could possibly reduce the dosage as well as frequency of taking medicine that they need.
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Detailed Description
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Study Aims \& Objectives:
The investigators' main goal is to apply a well defined simple exercise program that includes physical and breathing exercise lessons and evaluate its effects on the improvement of clinico-immunological outcome in obese patients with asthma. There are three main objectives based on clinic-immunological outcome.
1. To assess the improvement of asthma control, lung function and airways hyper-reactivity after the intervention.
2. To test if the proposed intervention will result in the improvement of pro-inflammatory profiles.
3. To determine if physical and psychological performances as well as health related quality of life are positively impacted by the proposed exercise modality.
About 200 individuals with asthma will be enrolled in this study and divided into two groups: The intervention group and controls. The intervention group will receive standard asthma care along with breathing/mild physical exercise. The control group will be the asthmatic patients who are not willing to receive the exercise intervention. At study entry, participants will undergo a clinical assessment which includes physical exam, asthma control/ quality of life questionnaires, pulmonary function tests, and lung inflammation test (Exhaled Nitric Oxide). To monitor participants throughout the study, follow up visits will be done at 6, 12, 18 and 24 weeks after starting the exercise. About 40 ml blood will be collected at baseline (pre-exercise) and two different time points (3 and 6 months of post-exercise). The blood samples will be used for pro-inflammatory profiles. Duration of the study will be three years.
Conditions
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Study Design
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NON_RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
NONE
Study Groups
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Interventional
Participants will receive standard asthmatic treatment and breathing/mild physical exercise
Exercise
Participants will perform 2-4 sessions of the prescribed exercise every day (One session: deep breathing 5-10 times; upper body stretching 5-10 times).
Control Arm
The control arm will receive standard medical care for asthma
No interventions assigned to this group
Interventions
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Exercise
Participants will perform 2-4 sessions of the prescribed exercise every day (One session: deep breathing 5-10 times; upper body stretching 5-10 times).
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Non-smokers and ex-smokers (should have stopped smoking at least 1 year ago)
Exclusion Criteria
* Inability to exercise
* Current smokers or those who stopped smoking within the last week
* Presence of other lung diseases besides asthma
* Patients on systemic steroids
* Major co-morbidities inhibiting participants from being involved in an exercise program
18 Years
ALL
No
Sponsors
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Dasman Diabetes Institute
OTHER
Responsible Party
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Rasheed Ahmad, PhD
Principal Investigator
Principal Investigators
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Rasheed Ahmad, PhD
Role: PRINCIPAL_INVESTIGATOR
Principal Investigator, Dasman Diabetes Institute
Fahad Al-Ghimlas, MD
Role: PRINCIPAL_INVESTIGATOR
Co-Principal Investigator, Dasman Diabetes Institute
Locations
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Dasman Diabetes Institute
Kuwait City, , Kuwait
Countries
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Other Identifiers
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RA-2011-015
Identifier Type: -
Identifier Source: org_study_id
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