- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02047370
Manual Therapy in Patients With Asthma
Effects of Manual Therapy in Patients With Asthma
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Asthma is a chronic lung disease involving an inflammation and a narrowing of the airways. Asthma causes wheezing, chest tightness, shortness of breath, and coughing.
A variety of manual therapies are commonly used to treat patients with asthma. There is a need to conduct studies in order to examine the effects of manual therapies on clinically relevant outcomes. Techniques aim to increase movement in the rib cage and the spine to try and improve the working of the lungs and circulation.
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
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Granada, Spain, 18071
- Faculty of Health Sciences. University of Granada
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Age ranging between 18 and 45 years.
- Diagnosis of asthma.
- No exacerbations during last month.
Exclusion Criteria:
- History of spine surgery.
- Diabetes, neurological or a cardiovascular disease.
- Spine deformities and use of orthopedic devices.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Single Group Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Diaphragm stretching
30 Patients with asthma are included in this group.
They will receive a diaphragm stretching technique
|
The therapist stands behind the patient and passes his hands around the thoracic cage, carefully introducing fingers under the costal margins.
The patient slightly rounds the trunk in order to relax rectus abdominis.
During the exhalation of the patient the therapist grasps the lower ribs and costal margin and eases the hands caudally.
This traction was maintained during 5-7 minutes.
Other Names:
|
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Placebo Comparator: Placebo group
Ultrasound disconnected in same position and with the same duration.
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The same therapist, patient position and duration of the technique, but using disconnected ultrasound
Other Names:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Forced vital capacity
Time Frame: Baseline, 7 days
|
The amount of air which can be forcibly exhaled from the lungs after taking the deepest breath possible.
It is going to be measured using a spirometer as recommended by the American Thoracic Society.
|
Baseline, 7 days
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Abdominal Kinematics
Time Frame: baseline, 7 days
|
Abdominal kinematic measurements can be used as an evaluative method to quantify possible alterations in abdominal movements.
|
baseline, 7 days
|
|
Airway diffusing capacity
Time Frame: baseline, 7 days
|
The airway diffusion capacity will be measure using the deep breeze device.
This is a non-invasive and radiation-free gadget that provides a dynamic image of the lungs, delivering both structural and functional information.
|
baseline, 7 days
|
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Forced expiratory volume in the first second
Time Frame: baseline, 7 days
|
This is the amount of air which can be forcibly exhaled from the lungs in the first second of a forced exhalation.
It is going to be measured using a spirometer as recommended by the American Thoracic Society.
|
baseline, 7 days
|
|
Rib cage excursion
Time Frame: baseline, 7 days
|
Rib cage excursion can be used as an evaluative method for diaphragmatic breathing excursion to quantify possible alterations in thoracic capacity and chest wall compliance as achieved by all expiratory and inspiratory muscles
|
baseline, 7 days
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- DF0046UG
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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-
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