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Mobile Applications clinical trials

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NCT ID: NCT06164041 Completed - Physical Activity Clinical Trials

Training and Detraining Effects of a Physical Activity Program Implemented Through Mobile Applications in Adolescents.

Start date: January 9, 2023
Phase: N/A
Study type: Interventional

The use of mobile applications to promote the practice of physical activity has begun to be used in the adolescent population in recent years. This has made it possible to carry out interventions inside and outside the educational setting, the latter being the ones that have brought the greatest benefits. Thus, it has been observed that the promotion of the use of mobile applications in out-of-school hours from the subject of physical education has reported significant benefits on body composition and fitness in the adolescent population. However, there is no known research that has analyzed whether the effect achieved with mobile applications when their use is mandatory disappears when they are no longer promoted from the physical education subject. Therefore, this project goes further and tries to find out whether after the ten-week period of mandatory use of the applications, adolescents continue to use the applications autonomously and the beneficial effects achieved are maintained or disappear due to the lack of use. For this purpose, a 10-week intervention was planned in which the adolescents used the mobile applications. Prior to the start of the intervention, the adolescents' body composition and fitness (pre) were measured. At the end of the intervention of mandatory use of the mobile applications, the adolescents were measured again (post). And after the post measurement, the adolescents were left for 10 weeks during which they could use the applications autonomously. A third measurement of the adolescents was performed after this 10-week period (post 2). The aim of this project was to find out the effects of stopping the use of the mobile fitness apps on body composition and fitness of the adolescents.

NCT ID: NCT05715541 Completed - Mobile Applications Clinical Trials

Inr Tracking Coumadin Use With Phone App

Start date: June 1, 2021
Phase: N/A
Study type: Interventional

This study aims to compare the INR values of the patients followed by face-to-face and telephone applications.

NCT ID: NCT05263726 Completed - Hypertension Clinical Trials

The Effect of a Disease Self-management Program Through a Mobile Applications for Patients With Hypertension

Start date: February 8, 2022
Phase: N/A
Study type: Interventional

Hypertension is a major cause of death worldwide. Patients should adjust their lifestyle and learn how to maintain a balance between self-management of a disease and their daily livelihood. Knowledge is networked, mobile devices can be used as a way of health education. The purpose of this study is to evaluation the effectiveness of the disease self-management program through a mobile applications for patients with hypertension. Statistical analyses was used analysis of covariance for checking the effect of interventions. Through the calculation by a statistical power analysis formula, the study takes 70 samples and divides them into a control group (usual care) and an experimental group (disease self-management program through a mobile applications) by the single blind randomized controlled trial, whereby each groups has 35 samples. The first step investigate the physiological indicators, mental health, self-management, quality of life of the patients. For the experimental group, after the pre-test the study set up a health guide for the disease self-management program with a mobile applications. The experimental group received the mobile apps educational program for at least 30 minutes each session and at least once every two days. After two weeks and six weeks, a follow-up telephone interview helped to strengthen the health self-management self-confidence. The effect of interventions was then evaluated after three months when the patients returned. Therefore, the self-management of a disease can be improved and patients will learn to live in harmony with hypertension by improving their mental health, self-management, and quality of life.

NCT ID: NCT05157919 Completed - Critical Care Clinical Trials

Mobile App to Promote Family Caregiver Engagement in the Intensive Care Unit

ICU-CARE
Start date: January 6, 2020
Phase: N/A
Study type: Interventional

The purpose of this randomized controlled pilot trial is to develop and test mobile app, Intensive Care Unit-Caregiver Activation Response, and Engagement (ICU-CARE). ICU-CARE provides a simulated learning environment to encourage family caregivers of mechanically ventilated patients to assess two patient symptoms, thirst and anxiety, and perform specific nonpharmacologic comfort measures to help alleviate patient symptom burden.

NCT ID: NCT04821518 Completed - Stroke Clinical Trials

The Use of Samsung Health and ECG M-Trace Base II Applications in the Secondary Prevention After Stroke

Start date: November 15, 2020
Phase:
Study type: Observational [Patient Registry]

The aim of the present study was to quantitatively assess the risk factors that may affect the re-occurrence of a CVD event and the use of a commercially available mobile application Samsung Health for the assessment of parameters of exercise tolerance and the ECG M-Trace Base II application for the assessment of cardiological parameters.

NCT ID: NCT04783324 Completed - Pregnant Women Clinical Trials

The Effect of the E-Mobile Health Application on Postpartum Adaptation

Start date: March 25, 2021
Phase: N/A
Study type: Interventional

The purpose of this research is to determine the effect of the e-mobile health application on postpartum adaptation. The study will consist of two groups: Experimental group and control group.

NCT ID: NCT04358172 Completed - Mobile Applications Clinical Trials

The Effectiveness of a Mobile Application in Educating Partial Denture Wearers

Start date: July 29, 2019
Phase: N/A
Study type: Interventional

A randomised control trial to evaluate the effect of a mobile application on partial denture wearers's dental knowledge, oral hygiene and denture hygiene. The null hypothesis of the study states that there will be no difference in dental knowledge, oral and denture hygiene among patients educated using the mobile application compared to those educated using the conventional method of verbal instructions accompanied by demonstrations on dental models.

NCT ID: NCT04259268 Completed - Mobile Applications Clinical Trials

Evaluation of the Quality of Preoperative Information Obtained Through Preanestes@s, a Web Based Application

Preanestes@s
Start date: February 7, 2020
Phase:
Study type: Observational

In this prospective and paired study, the investigators evaluate whether the preoperative information recorded through a web based questionnaire together with a virtual non face to face patient assessment based on the information recorded by the questionnaire and the electronic records of patients is of a comparable quality to that obtained with the traditional outpatient interview.

NCT ID: NCT04150354 Completed - Mental Health Issue Clinical Trials

Mental Health Symptom Monitoring Utilizing the Cogito Behavioral Analytic Platform

Start date: October 28, 2016
Phase: N/A
Study type: Interventional

The primary objective of this project is to test the acceptability and feasibility of a mobile application to facilitate mental health symptom monitoring and follow-up among Veterans. During the course of the study, the research application will be installed on participants' mobile phone. The application on the participants' phone will be recording data about their behavior. Participants will also be asked to complete bi-weekly surveys via the app.

NCT ID: NCT04081961 Completed - Mobile Applications Clinical Trials

Feasibility Study to Use Biosensing Devices to Monitor PA and Resp. Function in Smokers w and w/o Resp. Symptoms/COPD

Start date: June 7, 2019
Phase:
Study type: Observational

This study examines the feasibility and acceptability of using mobile applications and biosensing (mHealth) devices in detecting vitality parameters in current smokers with and without respiratory symptoms/COPD (e.g., heart rate, blood oxygenation, steps/motion) for a future big-scale study.