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Breathing, Mouth clinical trials

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NCT ID: NCT06061497 Recruiting - Asthma Clinical Trials

Effectiveness of the Rehabilitation Nursing Consultation for People With Asthma on Symptom Control and Quality of Life

Start date: July 3, 2023
Phase: N/A
Study type: Interventional

Introduction Asthma is a chronic inflammatory disease of the respiratory airways and is considered a Public Health problem, which lacks a personalized multidisciplinary intervention, to allow the user to develop mastery in the self-management of his disease. The project intends to answer the question: What methods could be used to enhance the use of asthma controller therapy? Methods Randomized and controlled clinical trial. The sample consists of users with asthma at Family Health Units in the municipality of Oliveira de Azeméis. There will be an experimental group that will undergo structured rehabilitation nursing consultations, and a control group that will receive the usual nursing care appropriate for asthma management. Both groups will be subject to two evaluation moments with the CARAT test and the AQLQ-M questionnaire. Results The aim is to evaluate the effectiveness of interventions for people with asthma implemented within the framework of a structured rehabilitation nursing consultation. The investigators expected to observe a clinically significant improvement with regard to disease control, quality of life, and user empowerment.

NCT ID: NCT05987982 Recruiting - Pneumonia Clinical Trials

Mouth Odor on Preventing Pneumonia by Oral Frailty

Start date: August 14, 2023
Phase: N/A
Study type: Interventional

This research plan aims to first collect data on the oral function and oral hygiene status of the elderly population in the community and to understand the normal model of oral frailty among the older adults in the community. Subsequently, a comparison will be made between the oral status of hospitalized patients and the community-dwelling elderly population. The goal is to verify whether oral odor can be used as an objective biological indicator following intervention.

NCT ID: NCT05744765 Completed - Breathing, Mouth Clinical Trials

Effects of Breathing Exercises on Reaction Time

Start date: December 20, 2022
Phase: N/A
Study type: Interventional

The aim of the study was to investigate the short and long-term effects of breathing exercises on reaction time.

NCT ID: NCT05246930 Active, not recruiting - Asthma Clinical Trials

Evaluating the Use of a Device Called Impulse Oscillometry in Participants With Vocal Cord Disorders or Asthma

Start date: June 15, 2022
Phase:
Study type: Observational

This study will determine if airway resistance to airflow and pressure, measured by Impulse Oscillometry, is impacted in subjects with vocal cord disorders and whether these measurements are different when compared to subjects with asthma.

NCT ID: NCT05115097 Recruiting - COVID-19 Clinical Trials

AI Evaluation of COVID-19 Sounds (AI-EChOS)

AI-EChOS
Start date: September 20, 2021
Phase:
Study type: Observational

In this study the investigators record sounds of voice, breaths and cough of subjects who tested positive for COVID19. The investigators then feed these sounds into an artificial intelligence and see if it can learn to recognise features to make COVID19 diagnosis from these sounds in order to avoid to use swabs to test the general population.

NCT ID: NCT05085795 Completed - Clinical trials for Lung Function Decreased

Evaluating Deep Breathing in Health Participants Using a Device Called Impulse Oscillometry

Start date: October 4, 2021
Phase:
Study type: Observational

This study will determine if resistance of the airway to airflow and pressure, measured by Impulse Oscillometry, is impacted by a deep breathe maneuver in a small cohort of healthy human subjects.

NCT ID: NCT04776122 Completed - Breathing, Mouth Clinical Trials

Usability of a Breathing-CBT Platform (CBT = Cognitive Behavioural Therapy)

Start date: June 1, 2018
Phase: N/A
Study type: Interventional

The study will examine the usability of a breathing platform in the home environment. It will be a randomized, open-label crossover study of 10 participants who will complete the CBT and breathing components in their home, prior to sleeping. Usability will be measured by scores assigned by participants. Qualitative feedback and compliance information will also be collected.