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Primary Care clinical trials

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NCT ID: NCT03358433 Recruiting - Depression Clinical Trials

Effectiveness of Exercise in the Treatment of Depression

DEP-EXERCISE
Start date: June 1, 2016
Phase: N/A
Study type: Interventional

The main objective is to test the non-inferiority of supervised exercise versus antidepressant treatment in reducing depressive symptoms in patients with clinical criteria for depression (according to ICD 10) over a period of 6 months follow-up.

NCT ID: NCT03302572 Recruiting - Clinical trials for Randomized Controlled Trial

Effectiveness Brief Information Advanced Directives Primary Care

Start date: November 3, 2016
Phase: N/A
Study type: Interventional

The knowledge and completion of advanced directives (ADs) by the population is generally low. Primary care could develop a very important role to inform and assist in the preparation of this document because of its accessibility. Objective: To evaluate the effectiveness of an oral brief information and a brochure administered in primary care to improve the proportion of ADs records. Design: Randomized clinical trial. Ambit: 7 offices from a urban health center which serves about 25,000 users older than 18 years. Material and methods It will be administered randomly triptych and oral brief information about the existence of advance directives for people over 18 to attend the appointment of their family doctor for any reason (intervention group). It will be given the possibility of more extensive information if they wish and collaboration will be offered for the advance directive according to patient preferences. The control group will not receive any information. Follow-up: 3 months. Variables will be: number of people interested in ADs, number of ADs made and demographic data (gender, age, education level, race, comorbidities, religion, testament) in both groups. Statistical analysis: multiple linear regression, Poisson and Cox as response analyzed, with the intervention/control group as the main variable adjusting for potential confounders. Bivariate comparison using Student t test or Mann-Whitney test (continuous variables) and chi-square or Fisher's exact test (categorical variables). 165 subjects were required in the control group and 165 in the intervention group. Conclusion: positive results of this study will bring out the brief information managed by family physicians increases the number of ADs thus facilitating the right to autonomy of the patient.

NCT ID: NCT03267706 Not yet recruiting - Palliative Care Clinical Trials

Introducing the Palliative Care Comprehensive Tool in Family Medicine

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

The purpose of this study is to pilot the introduction of a newly developed palliative care tool to clinicians in a family health team. The intent of the tool is to improve the quality and comprehensiveness of palliative care, which effects caregiver and patient satisfaction with care received, as well as clinician satisfaction with their delivery of care. Tool effectiveness will be evaluated by measuring satisfaction scores of caregivers, patients and clinicians who receive training and access to the tool compared to caregivers, patients and clinicians providing usual care (without the tool). Uptake of the tool and user feedback will be collected

NCT ID: NCT03247049 Completed - Clinical trials for Intracerebral Hemorrhage

Prognosis in Intracerebral Hemorrhage. The ICHCat Score in Primary Care.

ICHCat
Start date: July 27, 2015
Phase: N/A
Study type: Observational [Patient Registry]

The clinical evidence shows that patients with a first episode of intracerebral hemorrhage (ICH) are increasingly old and with greater comorbidity with a recognized impact over mortality. The prediction of the outcome of ICH is not only crucial in the emergin attention to identify those patients with favorable criteria that can benefit from possible treatments; but also after hospital discharge, in primary care where the prediction should facilitate the organization and management of a wide variety of resources: familiar, health and social welfare. Even though there are different scales that predict mortality, these are not sufficiently useful in choosing a treatment or do not provide sufficient data to the family to decide. Due to the characteristics of the population with ICH described in these works, it seems useful to propose a prognostic index (ICHCat) to identify the variables associated to its incidence and mortality and that, in addition, to make adjustments in the comparisons of the survival between different series of patients or different treatment modalities in primary care.

NCT ID: NCT03135561 Completed - Physical Activity Clinical Trials

A Pedometer-based Intervention With and Without Email Counselling in General Practice

Start date: November 12, 2015
Phase: N/A
Study type: Interventional

A two-arm parallel randomised controlled trial comparing pedometer-based intervention with and without email counselling in a primary care setting. Physically inactive patients from four general practices will be randomised to the pedometer-plus-email group or to the pedometer-alone group. All patients will be instructed to gradually increase the daily number of steps to at least 10,000. Patients in the pedometer-plus-email group will receive 8 counselling emails based on behavioural techniques. The primary outcome will be change in average daily steps measured during 7-day period at baseline and at 12 weeks.

NCT ID: NCT02906423 Completed - Palliative Care Clinical Trials

Results From a Health System-wide Implementation of a Quality of Life Questionnaire

Start date: July 2012
Phase: N/A
Study type: Observational

The purpose of this retrospective chart review pilot study is to research the results and scores of the QOL questionnaire implemented across Allina Health clinics. This study will investigate average QOL scores by clinical population and demographic group, the change in scores over time, and the effect of clinical interventions on QOL scores. The results will provide insight into QOL trends within different patient populations and provide guidance regarding optimal treatment plans so that Allina caregivers can positively impact patients' QOL.

NCT ID: NCT02723916 Completed - Primary Care Clinical Trials

Parent Training in Pediatric Care: A Self Directed Tablet-Based Approach

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

High quality and effective parenting in the preschool years is connected with long term positive child behavior and mental health outcomes. The purpose of the study, "Parent Training in Pediatric Primary Care: A Self-directed Tablet-based Approach," is to test the outcomes and implementation of a tablet-based parent training program in Pediatric Primary Care. Testing and evaluating the implementation of digitally delivered programs is important to increase the ease, reach, sustainability, and integration of mental health prevention into primary care settings.

NCT ID: NCT02115412 Completed - Diabetes Mellitus Clinical Trials

Validation of Medication Non-adherence Model (UK)

Start date: July 2014
Phase:
Study type: Observational

Research has shown that nearly 50% of patients with chronic conditions around the globe do not adhere to their prescribed medicine, leading to enormous cost to the healthcare providers. Non-adherence can be due to various forms and have multiple causes. To address this need, Philips Research has developed Medication Non-adherence model. This tool will help in developing a systemic way of assessing medication non-adherence and providing decision support for targeted intervention to healthcare professionals. The aim of this study is to validate this model with 750 chronically ill patients in UK.

NCT ID: NCT02094040 Completed - Frailty Clinical Trials

Municipality-based Post-discharge Follow-up Visits

Start date: February 2012
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether discharge follow-up visit by primary physician and community-based nurse affects the risk of early re-hospitalisation among high risk older people discharged from a medical ward.

NCT ID: NCT02015845 Terminated - Primary Care Clinical Trials

Evaluation of Accuvein in Obese Patients

AVO
Start date: November 2013
Phase: N/A
Study type: Interventional

The objective of this study is to evaluate the effectiveness of Accuvein to facilitate placement of peripheral intravenous catheters in obese patients. This clinical protocol is designed to determine whether using Accuvein increases the ease and efficiency of venous cannulation (as perceived by the operator), decreases the time to effective cannulation, and decreases the patient's perception of the pain.