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Patient Compliance clinical trials

View clinical trials related to Patient Compliance.

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NCT ID: NCT01174706 Completed - Clinical trials for Medication Adherence

Impact of Information Prescriptions on Medication Adherence in Emergency Department (ED) Patients

Start date: November 2010
Phase: N/A
Study type: Interventional

The main objectives of this research are: 1. To identify factors that influence medication adherence rates in Emergency Department (ED) patients. 2. To measure the effects of alternative information prescriptions on medication adherence rates of ED patients. 3. To measure the effects of alternative information prescriptions (IRxs) on health and service utilization.

NCT ID: NCT01082523 Completed - Acne Clinical Trials

"A Randomized, Controlled, Evaluator-blinded Pilot Study to Evaluate the Effect of Automated Text Message Reminders on Patient Compliance With Topical Medications and Its Efficacy on Skin Disease Control in Adolescents and Adults With Mild to Moderate Acne"

Start date: February 2010
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether an automated electronic reminder system using text messages sent to patient's cell phones will help patients with acne be more compliant with their topical medications and lead to an improvement of their acne. Hypothesis: Automatically delivered electronic reminders in the form of text messages will increase acne patient adherence to topical medications and consequently result in better treatment outcome and higher patient satisfaction

NCT ID: NCT00944788 Completed - Quality of Life Clinical Trials

A Structured Qi-gong Program for Hospitalized Older Adults

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

The purpose of this study is to test the effects on a number of health outcomes and the feasibility of a structured program of qi-gong, a form of tai-chi which has been previously tested in older populations, in older hospitalized patients. In particular, this pilot study aims to assess changes in quality of life and depressive symptoms after 4 weeks of treatment, with the hypothesis that this intervention will have a positive impact on these two domains, compared to usual care. Adherence will be also monitored in the intervention arm.

NCT ID: NCT00679198 Completed - Osteoporosis Clinical Trials

Improving Osteoporosis Care in High-Risk Home Health Patients

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

SPECIFIC AIMS: We propose a three-year study to develop a high-intensity intervention to improve osteoporosis care and test a novel intervention in a group-randomized trial of 27 home health offices and 1,000 patients referred to home health care with a history of fracture. Aim 1. Develop an intervention to promote osteoporosis treatment that includes: (1) training to enhance nurse-patient and nurse-physician risk communication regarding osteoporosis and fracture risk; (2) automated prompts within the home health agency's electronic medical record system to promote appropriate osteoporosis management; and (3) implementation of osteoporosis-related standardized care pathways and order sets. Aim 2. Conduct a group-randomized trial to test the effectiveness of the intervention to promote initial use of osteoporosis medications and adherence to treatment after discharge from home health. We hypothesize that: H1: Patients in the intervention group will have increased initial receipt of osteoporosis prescription medications and calcium/vitamin D supplements to prevent and treat osteoporosis compared to patients receiving usual care; H2: Patients in the intervention group will demonstrate increased persistence in the use of these therapies compared to those receiving usual care. Secondary Aims (SA) will include exploratory analyses of fracture related morbidity and mortality, patient-reported quality of life, and health services utilization and costs.

NCT ID: NCT00459368 Completed - Asthma Clinical Trials

Using Information Technology to Improve Asthma Adherence

AFFIRM
Start date: May 2007
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether providing patient medication adherence information on inhaled corticosteroid use to clinicians will result in improved patient adherence and asthma control.

NCT ID: NCT00433134 Completed - Clinical trials for Kidney Transplantation

Survey of Adherence to Immunosuppression and Other Medications in Kidney Transplant Patients

Start date: June 2006
Phase: N/A
Study type: Observational

Goal: To define the causes and issues associated with nonadherence in our population Hypothesis: There is a difference in the rates and patterns of adherence to transplant medications versus other medications also taken by transplant patients Methods: 1. A standardized interviewer-administered confidential survey exploring levels of adherence to transplant medications and other medications as well questionnaires on a variety of cognitive and other factors known to be associated with adherence. 2. A brief review of demographics and pertinent laboratory information at the same encounter

NCT ID: NCT00229554 Completed - Clinical trials for Colorectal Neoplasms

Survey of ColoRectal Cancer Education and Environment Needs

SCREEN
Start date: March 2006
Phase: N/A
Study type: Observational

Despite strong evidence for the effectiveness and cost-effectiveness of a variety of colorectal cancer (CRC) screening methods for reducing CRC mortality, current CRC screening rates fall far below the levels needed to significantly impact CRC mortality. Unfortunately, however, the existing literature on patient CRC screening behavior does not yet provide a sufficient evidence base for making sound recommendations regarding how to most effectively improve upon these rates in the VA. This study will inform future CRC screening promotion efforts and make important scientific contributions to existing literature by: (a) delineating the relative contribution of patient cognitive, environmental and background factors to CRC screening behavior using a multi-level, theory driven analysis approach on a nationally representative sample, and (b) identifying the determinants of variation in CRC screening behavior across vulnerable population subgroups.