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Health Promotion clinical trials

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NCT ID: NCT05482685 Not yet recruiting - Health Promotion Clinical Trials

The Health-Promoting Behavior and Related Factors Among Home Care Attendants

Start date: July 30, 2022
Phase:
Study type: Observational

Background: With the trend of aging population and increasing demand for long-term care, Taiwan's long-term care 2.0 policy places special emphasis on home care services to achieve the goal of local aging. This study focused on the health-promoting behaviors home care attendants and applied Pender's health promotion model theory to investigate the impact of home care attendants' self-perceived health and health literacy on health-promoting behaviors. Objective: To investigate the current status of home care attendants' health-promoting behaviors and the correlation between self-perceived health and health literacy. Methodology: A structured questionnaire was used to collect data from 150 eligible home care attendants in the northern region using self-perceived health, health literacy, and health-promoting behaviors scales. Multiple regression analysis was used to analyze the correlation between the independent variables and the dependent variables. Expected contribution: The results of this study will help to understand the current status of health-promoting behaviors of home care attendants and the correlation with their self-perceived health and health literacy. It will also help to understand whether home care attendants have sufficient health literacy to maintain or improve their health status, and to understand the areas in which home care attendants' health-promoting behaviors are still inadequate, so as to suggest effective methods or strategies to improve health-promoting behaviors in the future.

NCT ID: NCT05460663 Completed - Health Promotion Clinical Trials

Improving Air Force Resilience

Start date: December 4, 2020
Phase: N/A
Study type: Interventional

The purpose of this study is to examine the effectiveness of the Stress Management and Resilience Training (SMART) in increasing resilience in Air Force (AF) healthcare personnel. SMART includes practices that focus on six factors that promote individual-level resilience. A pretest-posttest, randomized control trial will be used to examine the effectiveness of SMART and is guided by the Defense Centers of Excellence Resilience Continuum. After institutional review board approval, the principal investigator (PI) will recruit a sample of AF healthcare personnel assigned to the 88th Medical Group or USAF School of Aerospace Medicine at Wright Patterson AF Base. SMART will be provided via either a two-hour, video teleconference (VTC) or in-person training or a self-paced, on-line version completed over four to eight weeks. VTC or on-line versions will be utilized to prevent transmission of severe acute respiratory syndrome coronavirus-2. If in-person training is feasible and safe at a future point in time, in-person training will replace VTC training. A baseline survey will include questions regarding age, gender, marital status, race, ethnicity, previous deployment, military rank, and military job duty. The Connor Davidson 10-Item Resilience Scale has demonstrated reliability and validity, and has been used in studies to measure service member resilience. Additional measures include the Perceived Stress Scale, Generalized Anxiety Disorder Scale, and a Quality of Life measure. The CD-10, PSS, GAD-7, and QoL measure will be readministered 12, 18, and 24-weeks after SMART completion. Initial analysis will include descriptive statistics to characterize demographics, military grade, duty location, and previous deployment status. Cronbach's α will be calculated for each scale. Analyses will be reported as point estimates with 95% confidence intervals and estimates of effect size. Both VTC and on-line groups will be analyzed separately and scores will be pooled to test for overall intervention effects. The investigators will conduct regression models on the pre-post intervention difference while controlling for demographic characteristics and previous deployment. The investigators will consider clustering effects among participants from the same organizational unit using random effects. Changes in resilience, stress, anxiety, and QoL over time will be assessed by analyzing changes from baseline to weeks 12, 18, and 24. The investigators will consider a joint analysis of resilience, stress, anxiety, or QOL.

NCT ID: NCT05403060 Completed - Feeding Behavior Clinical Trials

Educational Nutritional Intervention for Adolescents

Start date: March 1, 2022
Phase: N/A
Study type: Interventional

Randomized controlled trial by conglomerates whose objective is to evaluate the effectiveness of an educational nutritional intervention, based on the Social Cognitive Theory, for the increase in the consumption of vegetables and fruits and the decrease in the consumption of ultra-processed foods in adolescent high school students, in the University of Guadalajara, in Guadalajara, Jalisco.

NCT ID: NCT05395364 Completed - Obesity Clinical Trials

A Health Promotion Intervention for Vulnerable School

BeE-school
Start date: March 1, 2022
Phase: N/A
Study type: Interventional

The BeE-school (Be Empowered in school) is a cluster-randomised trial that addresses the complexity of the social challenge (vulnerable school-age children). It aims to analyse the effectiveness of the intervention program, based on the promotion of health literacy and lifestyles, specifically on children's: 1-health literacy and infodemic resilience (Aim 1); 2- lifestyles (e.g. dietary intake, 24hmovement behaviour) (Aim 2); 3-overweight and obesity (Aim 3); 4-blood pressure (Aim 4). The project converges multiple disciplines (e.g. public health, informatics, law) and researchers with proven expertise in these fields to provide comprehensive and innovative answers. 478 children (6 schools) aged 6-12years old will participate in this cluster-randomised trial, having schools as the unit of randomisation, assigned into intervention (239-3schools) and the control arm (239 - 3 schools). This project will perform a social listening (online and offline) and bottom-up approach to tackling NCDs, focusing on health literacy and health promotion and recognising children's systems in daily life (e.g. family, teachers). Stakeholders' involvement goes far beyond a merely consultative approach; the researchers are committed to a genuine codevelopment process. Data collection includes sociodemographics, health literacy and infodemic resilience, dietary intake and children's 24-h movement behaviour (e.g. accelerometry), anthropometry (e.g. weight, height and waist circumference) and blood pressure. Data collection will occur at baseline and after the intervention (follow-up, 6 months after the beginning of the intervention). Expected outputs and outcomes include the creation of a model for characterising NCDs and health topics based on artificial intelligence techniques (e.g. deep learning, and social network analysis methods); improved health literacy and infodemic resilience of children, families and teachers; enhanced children's lifestyles (e.g. dietary intake, 24-h movement behaviour); reduction of NCDs' physical risk factors (e.g. overweight, raised blood pressure); feasible intervention program about health promotion and NCDs' prevention for school-aged children with vulnerabilities, and advocacy- policies about health promotion and NCDs' prevention.

NCT ID: NCT05333484 Completed - Exercise Clinical Trials

12-week Pilates Program on Community-dwelling Middle-aged Women

Start date: March 1, 2013
Phase: N/A
Study type: Interventional

The purpose of this study was to investigate the effects of a Pilates exercise intervention program on functional physical fitness in community-dwelling middle-aged women.

NCT ID: NCT05329207 Not yet recruiting - Health Promotion Clinical Trials

Effects of Web-Based Adolescent Health Promotion Program in Hearing Impaired Adolescents

ASGE-FABES
Start date: April 18, 2022
Phase: N/A
Study type: Interventional

Our research is to evaluate the effect and applicability of the adolescent health promotion program, which includes multiple behavioral interventions, on physical activity, nutrition and mental health of hearing impaired adolescents living in the community.

NCT ID: NCT05149443 Completed - Physical Activity Clinical Trials

Move it, Move ID! Promotion of Physical Activity in Adolescents With Intellectual Disability

Start date: January 1, 2022
Phase: N/A
Study type: Interventional

The aim of this study is to develop and implement an mHealth intervention focusing on the promotion of physical activity in adolescents with intellectual disability.

NCT ID: NCT05012163 Completed - Influenza Clinical Trials

Lottery Incentive Nudges to Increase Influenza Vaccinations

Start date: September 4, 2021
Phase: N/A
Study type: Interventional

In the current study, the study team will explore whether small incentives are effective at promoting flu vaccine uptake. The study is designed to compare the relative efficacy of incentives of equal perceived expected value (EV) or equal implementation costs, to assess whether people are more likely to get vaccinated in response to lotteries with very high payoffs than to small certain cash payout or slightly higher-probability, more moderate payoffs. In particular, given the potential appeal of official state lottery tickets, one study arm will receive a Pennsylvania scratch-off lottery ticket for getting a flu vaccine. A primary hypothesis is that lotteries will outperform simple reminders (encouraging respondents to get the flu shot at their upcoming appointment) and the standard of care, representing the ambient healthcare system and public health campaigns to increase vaccination.

NCT ID: NCT05009251 Completed - Influenza Clinical Trials

Using Explainable AI Risk Predictions to Nudge Influenza Vaccine Uptake

Start date: September 9, 2021
Phase: N/A
Study type: Interventional

The study team previously demonstrated that patients are more likely to receive flu vaccine after learning that they are at high risk for flu complications. Building on this past work, the present study will explore whether providing reasons that patients are considered high risk for flu complications (a) further increases the likelihood they will receive flu vaccine and (b) decreases the likelihood that they receive diagnoses of flu and/or flu-like symptoms in the ensuing flu season. It will also examine whether informing patients that their high-risk status was determined by analyzing their medical records or by an artificial intelligence (AI) / machine-learning (ML) algorithm analyzing their medical records will affect the likelihood of receiving the flu vaccine or diagnoses of flu and/or flu-like symptoms.

NCT ID: NCT05000619 Completed - Prevention Clinical Trials

Encouraging Overdue Healthcare Appointment Scheduling Among Patients With Chronic Diseases

Start date: July 12, 2021
Phase: N/A
Study type: Interventional

The goal of this study is to determine the most effective messages for encouraging patients with chronic conditions, who have not seen their doctor in at least one year, to return to the clinic. Study participants will receive postcards or letters encouraging them to make an appointment. Researchers will assess whether messages increase appointment scheduling (and attendance).