Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04737824
Other study ID # ESS-Balloon
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 1, 2021
Est. completion date March 31, 2021

Study information

Verified date August 2021
Source Escola Superior de Tecnologia da Saúde do Porto
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Despite the literature evidence that the "balloon-blowing exercise" improves the pulmonary function as a long-term effect, this exercise has not yet been studied or tested experimentally, meaning that there are no specific and measurable results that attest the improvement on thoracoabdominal movement.


Recruitment information / eligibility

Status Completed
Enrollment 42
Est. completion date March 31, 2021
Est. primary completion date March 31, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 25 Years
Eligibility The target population consisted of healthy physiotherapy students from School of Health - Polytechnic of Porto, who volunteered to participate in study. Inclusion criteria: - In the Experimental Group B were admitted individuals that, through the analysis of the training record sheet, had executed 2/3 of the programmed sessions. Exclusion criteria: - Individuals that had participated in aerobic physical activities of moderate (i.e., at least 30 minutes on five days per week) or vigorous intensity (i.e., at least 20 minutes on three days per week) for more than one year; - Chronic nonspecific lumbopelvic pain (i.e., recurrent episodes of lumbopelvic pain for a period exceeding three months); - Flu symptoms or respiratory infection up to one week before data collection; - History of recent ribs fracture and pain in the last three months; - Pulmonary or rib cage previous pathologies; - Length discrepancy of the lower limbs or other postural asymmetries; - History of spinal, gynaecological, or abdominal surgery in the previous year; - Recurrent muscle/joint pain and history of musculoskeletal injury in the last three months; - Smoking and/or drinking habits.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
An adaptation of the "balloon-blowing" exercise
The participants were positioned in supine, on a semi-rigid surface, with the upper limbs placed above the level of the head, at rest. Their feet were also placed at a resting position on a wall and with their hips and knees at 90o of flexion. The cervical was placed in a neutral position and the pelvis was maintained in a posterior pelvic tilt, both structures corrected by the researcher. The participants were asked to contract the adductors, maintaining a bilateral and symmetric pressure between 10 and 15 mmHg on two sphygmomanometers placed between the knees. Also, an isometric contraction of the hamstrings and gluteus was requested. A Threshold®, with a minimum resistance of 5 cmH2O, and they were instructed to close their lips around the mouthpiece, to avoid air leaks. To start the exercise, it was transmitted to the participants to make a maximum inspiration through the nose, for two seconds. Subsequently, a maximum exhalation throughout the threshold was made for three seconds.
An adaptation of the "balloon-blowing" exercise for seven weeks, three times a week, at home
The participants were positioned in supine, on a semi-rigid surface, with the upper limbs placed above the level of the head, at rest. Their feet were also placed at a resting position on a wall and with their hips and knees at 90o of flexion. The cervical was placed in a neutral position and the pelvis was maintained in a posterior pelvic tilt, both structures corrected by the researcher. The participants were asked to contract the adductors, maintaining a bilateral and symmetric pressure between 10 and 15 mmHg on two sphygmomanometers placed between the knees. Also, an isometric contraction of the hamstrings and gluteus was requested. A Threshold®, with a minimum resistance of 5 cmH2O, and they were instructed to close their lips around the mouthpiece, to avoid air leaks. To start the exercise, it was transmitted to the participants to make a maximum inspiration through the nose, for two seconds. Subsequently, a maximum exhalation throughout the threshold was made for three seconds.

Locations

Country Name City State
Portugal Escola Superior de Saúde - Instituto Politécnico do Porto Porto

Sponsors (1)

Lead Sponsor Collaborator
Escola Superior de Tecnologia da Saúde do Porto

Country where clinical trial is conducted

Portugal, 

References & Publications (3)

Boyle KL, Olinick J, Lewis C. The value of blowing up a balloon. N Am J Sports Phys Ther. 2010 Sep;5(3):179-88. — View Citation

De Troyer A. Respiratory effect of the lower rib displacement produced by the diaphragm. J Appl Physiol (1985). 2012 Feb;112(4):529-34. doi: 10.1152/japplphysiol.01067.2011. Epub 2011 Dec 1. — View Citation

Key J. 'The core': understanding it, and retraining its dysfunction. J Bodyw Mov Ther. 2013 Oct;17(4):541-59. doi: 10.1016/j.jbmt.2013.03.012. Epub 2013 Jun 28. Review. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Anterior-to-posterior movement of the upper rib cage Thoracoabdominal movement was measure through "Qualisys motion capture system". Immediate after procedure
Primary Anterior-to-posterior movement of the lower rib cage Thoracoabdominal movement was measure through "Qualisys motion capture system". Immediate after procedure
Primary Anterior-to-posterior abdominal movement Thoracoabdominal movement was measure through "Qualisys motion capture system". Immediate after procedure
Primary Medial-to-lateral movement of the upper rib cage Thoracoabdominal movement was measure through "Qualisys motion capture system". Immediate after procedure
Primary Medial-to-lateral movement of the lower rib cage Thoracoabdominal movement was measure through "Qualisys motion capture system". Immediate after procedure
Primary Anterior-to-posterior movement of the upper rib cage Thoracoabdominal movement was measure through "Qualisys motion capture system". Seven weeks
Primary Anterior-to-posterior movement of the lower rib cage Thoracoabdominal movement was measure through "Qualisys motion capture system". Seven weeks
Primary Anterior-to-posterior abdominal movement Thoracoabdominal movement was measure through "Qualisys motion capture system". Seven weeks
Primary Medial-to-lateral movement of the upper rib cage Thoracoabdominal movement was measure through "Qualisys motion capture system". Seven weeks
Primary Medial-to-lateral movement of the lower rib cage Thoracoabdominal movement was measure through "Qualisys motion capture system". Seven weeks
See also
  Status Clinical Trial Phase
Recruiting NCT06052553 - A Study of TopSpin360 Training Device N/A
Completed NCT05511077 - Biomarkers of Oat Product Intake: The BiOAT Marker Study N/A
Recruiting NCT04632485 - Early Detection of Vascular Dysfunction Using Biomarkers From Lagrangian Carotid Strain Imaging
Completed NCT05931237 - Cranberry Flavan-3-ols Consumption and Gut Microbiota in Healthy Adults N/A
Completed NCT04527718 - Study of the Safety, Tolerability and Pharmacokinetics of 611 in Adult Healthy Volunteers Phase 1
Terminated NCT04556032 - Effects of Ergothioneine on Cognition, Mood, and Sleep in Healthy Adult Men and Women N/A
Completed NCT04065295 - A Study to Test How Well Healthy Men Tolerate Different Doses of BI 1356225 Phase 1
Completed NCT04107441 - AX-8 Drug Safety, Tolerability and Plasma Levels in Healthy Subjects Phase 1
Completed NCT04998695 - Health Effects of Consuming Olive Pomace Oil N/A
Completed NCT01442831 - Evaluate the Absorption, Metabolism, And Excretion Of Orally Administered [14C] TR 701 In Healthy Adult Male Subjects Phase 1
Terminated NCT05934942 - A Study in Healthy Women to Test Whether BI 1358894 Influences the Amount of a Contraceptive in the Blood Phase 1
Recruiting NCT05525845 - Studying the Hedonic and Homeostatic Regulation of Food Intake Using Functional MRI N/A
Completed NCT05515328 - A Study in Healthy Men to Test How BI 685509 is Processed in the Body Phase 1
Completed NCT04967157 - Cognitive Effects of Citicoline on Attention in Healthy Men and Women N/A
Completed NCT05030857 - Drug-drug Interaction and Food-effect Study With GLPG4716 and Midazolam in Healthy Subjects Phase 1
Recruiting NCT04494269 - A Study to Evaluate Pharmacokinetics and Safety of Tegoprazan in Subjects With Hepatic Impairment and Healthy Controls Phase 1
Recruiting NCT04714294 - Evaluate the Safety, Tolerability and Pharmacokinetics Characteristics of HPP737 in Healthy Volunteers Phase 1
Completed NCT04539756 - Writing Activities and Emotions N/A
Recruiting NCT04098510 - Concentration of MitoQ in Human Skeletal Muscle N/A
Completed NCT03308110 - Bioavailability and Food Effect Study of Two Formulations of PF-06650833 Phase 1