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Health Education clinical trials

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NCT ID: NCT03303287 Recruiting - Health Education Clinical Trials

School Health Education Program in Pakistan(SHEPP)

SHEPP
Start date: September 15, 2017
Phase: N/A
Study type: Interventional

Pakistan is a developing country and there have been a considerable rise in obesity and hypertension in children in recent years. In this setting a focus on primary prevention of cardiovascular diseases is more cost effective than spending resources on secondary or tertiary prevention,. Primary prevention includes interventions to promote physical activity (> 30 minutes/day in school), healthy dietary habits (decreased consumption of sweetened beverages and snacks, and increased consumption of fruit and vegetables) and health education focusing on cardiovascular risk factors in school children. This would translate into healthier cardiovascular outcomes (eg. less hypertension, dyslipidemia and diabetes) in adult life. The investigators propose a school health education program for Pakistan (SHEPP) for children aged 9-11 years in 3 schools in Karachi for a period of one year. This program will comprise of 140 minutes physical activity/week (including aerobics):30 minutes aerobic PA(30*2=60) + 10 minutes (10*5=50)physical activity in assembly daily+ 1 minute between periods(1*6*5=30) and healthy diet and healthy heart teaching. Additionally teaching will also be given to teachers and parents, who will further reinforce these habits in children. We hypothesise that SHEPP will improve physical activity levels, dietary habits and knowledge about healthy heart in children, will decrease blood pressure, body mass index, waist circumference, at the end of the year. If this healthy behavior is carried on to adult life it will serve as an excellent primary prevention measure. The investigators , later on plan to study long term outcomes after implementation of this intervention.

NCT ID: NCT03125668 Completed - Quality of Life Clinical Trials

Impact of Telephone Follow-up in Patient's Health-related Quality of Life That Use Warfarin

Start date: October 1, 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to test an educational program with telephone follow-up to improve health-related quality of life (HRQoL), treatment adherence, and reduce anxiety and depression symptoms in patients who are starting oral anticoagulants (OA).

NCT ID: NCT03077464 Completed - Clinical trials for Health Knowledge, Attitudes, Practice

Behaviorally Oriented Nutrition Education at a Russian Summer Camp

Start date: June 1, 2014
Phase: N/A
Study type: Interventional

Healthful eating is a core component of a healthy lifestyle that is associated with lower risk of obesity and chronic disease. Although adolescent health promotion programs have been extensively evaluated and applied in English-speaking Western developed nations, there is very little published literature in the Russian context. Our study seeks to determine the relative effectiveness of a healthy lifestyle intervention consisting of nutrition education at a Russian camp. Investigators will determine the impact of behaviorally focused nutrition education on nutrition knowledge, food choice, attitude, and self-efficacy for healthful eating, compared to standard nutrition education.

NCT ID: NCT03051295 Completed - Health Education Clinical Trials

Dentists' Understanding of Diagnostic Test Results and Treatment Efficacy.

RCDENT2017
Start date: June 8, 2016
Phase: N/A
Study type: Interventional

There is little evidence on how best to present diagnostic and treatment effect information to dentists and whether this makes any difference to their understanding of the information given and clinical management. The objective of this study is to assess the influence of different formats for presenting diagnostic test results and treatment efficacy on dentists' understanding and on their reported clinical management. The hypothesis is that presenting diagnostic test and treatment effectiveness results using natural frequencies influences the threshold for treatment and improves interpretation of tests results compared to conditional probabilities and percentage differences. A group of dentists recruited from postgraduate courses were randomized to two of four arms, being two arms of a hypothetical realistic diagnostic scenario (a) and two arms of a hypothetical realistic treatment scenario (b): a1) diagnostic test results presented in conditional probabilities; a2) diagnostic test results presented in natural frequencies; b1) treatment efficacy presented in percentages; b2) treatment efficacy presented in natural frequencies. The main outcome measures were the correct answer as to whether disease was actually present (post-test probability) and the correct answer as the number of patients that would benefit from the treatment (efficacy). Secondary outcome measures included the decision whether to treat or not treat the hypothetical patient.

NCT ID: NCT02938676 Not yet recruiting - Clinical trials for Heart Transplantation

Satisfaction Degree in a Nurse Educational Program to Heart Transplant Patient

Start date: November 2016
Phase: N/A
Study type: Observational

Any member of the research team conducted screening for the selection of eligible patients. Nurses will be responsible for delivering the "Guide tips for the person with a transplanted heart", thus initiating an individualized education program. Education will be held at the time of admission in which the patient has passed the most critical post-operative. Educational tips guide contains all the information necessary for the patient to have a first contact on the habits that must change. Education lasts 10-30 minutes and is taught in daytime, in a calm environment and at the right time, favoring the presence of the caregiver. Later, education is reinforced on the doubts that arise both the patient and the primary caregiver. During the first days of admission to the unit of cardiology, socio-demographic data of the patient and primary caregiver by the research team will be collected. A few days before discharge, having left time between 7-8 days after delivery of educational advice guide, any member of the research team, who does not work in the cardiology unit, will provide the patient and the primary caregiver the satisfaction questionnaire where the perception of information and education received during the postoperative period in the inpatient cardiology unit and the appropriateness of the topics covered in the guide educational advice.

NCT ID: NCT02591511 Completed - Health Education Clinical Trials

Effects of Patient-centered Stroke Educating System: a Randomized Controlled Trial

Start date: October 2015
Phase: N/A
Study type: Interventional

The aim of this study is to establish PAtient-Centered Computerized Educating System for Stroke (PACCESS) for patients with different demands and lack of knowledge.Those in the intervention group will receive the PACCESS and the control groups will receive traditional health education to test the effects of PACCESS in increasing clinical decision-making, health behavior, activities of daily living and knowledge of stroke, and health care quality.

NCT ID: NCT01365026 Recruiting - Health Behavior Clinical Trials

PVS: Innovative Programs For Healthy Lifestyle Promotion in Primary Care: 'Prescribe Healthy Life'

PVS
Start date: January 6, 2016
Phase: N/A
Study type: Interventional

The potential health gains from healthy lifestyles are very well-known, what is still not known is how to help people to adopt these lifestyles, by means of brief interventions feasible in routine general practice. This study was designed to explore the feasibility and efficacy of innovative implementation strategies for the promotion physical activity, diet and smoking abstinence in primary care. The investigators hypothesize that collegiate planning between practitioners, researchers and managers, with a socio-ecological perspective and taking into account the real context of collaborating centers, will guarantee the sustainability and effectiveness of these programs.

NCT ID: NCT01014169 Completed - Health Education Clinical Trials

Study of the Impact of Parental Note Taking on the Effectiveness of Anticipatory Guidance

Start date: December 2009
Phase: N/A
Study type: Interventional

The delivery of anticipatory guidance is an essential component of pediatric practice. Given the large amount of information to be shared during each encounter and the limited time available, there is a need for an effective and efficient means of communication between health care providers and families. The investigators hypothesize that more active parental participation in the form of note taking during the delivery of anticipatory guidance will lead to increased knowledge, higher levels of satisfaction with the encounter, and increased adoption of recommended parenting practices. In this study, the investigators propose a randomized controlled trial of the impact of note taking during the delivery of newborn anticipatory guidance on maternal practices related to newborn care. The investigators plan to compare a control group of mothers receiving standard of care anticipatory guidance with an intervention group of mothers who are encouraged to take written notes while receiving the anticipatory guidance. The primary outcome of interest is maternal practice related to infant sleep position, and the secondary outcomes of interest are maternal practice related to breastfeeding initiation and car seat use. The investigators also plan to evaluate the impact of note taking on mothers' knowledge of recommended practices related to newborn care and on mothers' satisfaction with the guidance received.

NCT ID: NCT00425048 Completed - Hygiene Clinical Trials

Does Gloved Medical Personnel Scratch Less Often?

Start date: January 2007
Phase: N/A
Study type: Observational

Unconscious touching of a person's own head or neck (for example by scratching) is a frequently observed and completely normal physiological movement pattern in humans, which when done by medical personnel attending a patient poses a high risk of unconscious self-contamination, even of an already disinfected hand, and of subsequent contamination of the patient. However, as compared to an ungloved hand, a gloved hand is felt to be "foreign," which could reduce the frequency of self-contact and thus the contamination rate. Wearing protective gloves is highly recommended in medical practice. The purpose of this study is to explore how wearing, or not wearing, protective gloves affects - the frequency of unconscious self-contact - contamination of the gloved/ungloved hand