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Patient Compliance clinical trials

View clinical trials related to Patient Compliance.

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NCT ID: NCT02470650 Recruiting - Patient Compliance Clinical Trials

Cost-effectiveness of Different Antiretroviral Treatment in Patients HIV Naive

Start date: June 2015
Phase: Phase 4
Study type: Interventional

The main objective of this study is to know the efficiency (costeffectiveness) at 48 weeks of initiation of antiretroviral treatment. three strategies of treatment.

NCT ID: NCT02377960 Completed - Hypertension Clinical Trials

Check and Support -Enhancing the Treatment of Hypertension in Outpatient Care, a Multicenter Study

Start date: January 27, 2015
Phase: N/A
Study type: Interventional

The purpose of this pragmatic multi-centre, cluster randomized controlled trial is to test the effectiveness of tailored SMS-text message support combined with an information-motivation-behavioral skills (IMB) model-based initiation of medication in helping outpatient care patients with hypertension to achieve blood pressure target and to enhance medication adherence.

NCT ID: NCT02339597 Recruiting - Patient Compliance Clinical Trials

Therapy Adherence of APAP Therapy Initiation in Sleep-lab Versus at Home

Start date: January 2014
Phase: N/A
Study type: Interventional

Primary hypothesis: The objective compliance ( # of hours per night of APAP therapy) is higher in patients who get the APAP treatment initiation at home due to the fact that they get better support by telemetric control and the possibility of prompt interventions. Secondary hypothesis: Based on the higher support at the home APAP initiation the following parameters will be better in comparison to the standard supply in laboratory: Objective measures: - mask leakage - pressure - Apnea-Hypopnea-Index (AHI) Subjective measures: - quality of life - sleepiness

NCT ID: NCT02301923 Not yet recruiting - Clinical trials for Sleep Apnea, Obstructive

Continuous Positive Airway Pressure (CPAP) Compliance in Obstructive Sleep Apnea

CPAPcompl
Start date: November 2014
Phase: N/A
Study type: Observational

This study aims to determine the average compliance of a patient under CPAP therapy for obstructive sleep apnea as well as the various factors that influence it.

NCT ID: NCT02294019 Completed - Patient Compliance Clinical Trials

Actual Use Trial of Ibuprofen 400 mg

Start date: November 2014
Phase: Phase 3
Study type: Interventional

This is an open label, multicenter, 30 day study designed to mimic an OTC like environment in which subjects will use the product after making a purchase decision about ibuprofen 400 mg caplets based only on their reading of the Drug Facts Label (DFL) and other information on the package.

NCT ID: NCT01908517 Completed - Patient Compliance Clinical Trials

Human Papilloma Viruses (HPV) Vaccine Adherence Community Clinic Study

Start date: August 2013
Phase: N/A
Study type: Interventional

There has been very limited research that has looked at electronic reminders (text messages) and its effectiveness in adherence to vaccination among low-income minority populations. Results have shown that text messages, among low-income parents and adolescents who were identified as having a cellphone, is an effective strategy to increase the likelihood of adolescent vaccination adherence. Hard copy and electronic messaging reminders have also been proven to be effective when coupled with other prevention strategies for immunizations for influenza and pneumococcal pneumonia and screening for colon, breast, and cervical cancer in adults. Additionally, Merck and Co. recommend electronic reminders in their patient compliance program as a key strategy for adherence. To our knowledge, this community-based pilot intervention study will be the first to assess electronic reminders and HPV vaccine initiation and adherence among rural uninsured and Medicaid populations. The investigators hypothesize that adolescent whose parents who receive the intervention will be more likely to initiate HPV vaccination and be compliant at 3 months and at 7 months as compared to the control group.

NCT ID: NCT01897870 Completed - Patient Compliance Clinical Trials

The Effect of a Pharmacist Home Visit on Drug-related Problems Post-discharge.

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

the purpose of this study is to determine the the effect of a home-based medication management program on drug-related problems post-discharge.

NCT ID: NCT01837004 Completed - Patient Compliance Clinical Trials

Cognitive Regulation Training and Exercise

CORTEX
Start date: January 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to compare CORTEX (Cognitive Regulation Training and Exercise), a multi-faceted, general and exercise-specific cognitive training program plus a 4-month exercise program, to an attention-control condition involving health and wellness informational lectures plus videos. The proposed exercise program will involve both aerobic and resistive exercises. The investigators hypothesize that pre-intervention cognitive training will enhance self-regulation and self-efficacy and in turn, increase exercise adherence. The investigators also expect more positive improvements in cognitive and psychosocial function among participants in the CORTEX condition as compared to the Control condition immediately following the cognitive booster training, and across time.

NCT ID: NCT01807442 Completed - Clinical trials for Acute Coronary Syndrome

Positive Psychology to Improve Cardiac Health Behaviors

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

The purpose of the study is to understand peoples' positive emotions, like how optimistic or grateful they feel, after they have had a heart problem. The investigators want to determine whether positive emotions affect peoples' ability to follow recommendations, like following a healthy diet, exercising, and taking medication.

NCT ID: NCT01752595 Completed - Clinical trials for Myocardial Infarction

The Music Activity INTervention for Adherence Improvement Through Neurological Entrainment

MAINTAIN
Start date: November 2012
Phase: N/A
Study type: Interventional

Auditory motor-coupling has been shown to induce neural-entrainment that can synchronize walking-pace with sonic tempo. The extent to which acoustical-motor entrainment can induce longer-term changes to physical activity behaviours remains unclear. Cardiac rehabilitation is essential and is associated with irrefutable mortality benefits for patients following an acute cardiac event. Randomized clinical trials have demonstrated a 25-50% improvement in survival as compared to controls; however, as many as 50% of patients will dropout of such programs prior to completion, which undermines these morbidity and mortality benefits (37; 54). Research exploring ways to improve compliance to such programs has suggested that the incorporation of music and other such holistic, patient-centered interventions into a rehabilitation/exercise program is associated with improved motivation, endurance and satisfaction amongst cardiac rehabilitation participants. The MAINTAIN study has been designed to conduct a feasibility evaluation on the effects of a preference-based music intervention on adherence to the cardiac rehabilitation program at Toronto Rehabilitation Institute. The primary objective of the trial is to evaluate the feasibility of the implementation of such a protocol within the context of the program. This is a two-arm, block 2:1 randomized trial. 35 patients participating in cardiac rehabilitation at Toronto Rehabilitation: Cardiac Rehabilitation and Secondary Prevention Program will be recruited and participants will be randomized into: 1) control (standard, usual care); and, 2) music intervention. The randomization process employed will be a blocked 2:1 strategy, whereby subjects are randomized to the music treatment arms 2:1. All those patients randomized into arm 2 will be equally randomized into either (2) preference-based music intervention, (3) preference-based music enhanced with RAS. The primary outcome measure will be weekly physical activity over a 3 month duration as measured using tri-axial accelerometers. We will also analyze the impact of a preference-based music intervention based on audio playlist utilization, self-reported sitting times ,exercise-times, on-site attendance to the cardiac rehabilitation program (attendance), peak oxygen uptake (VO2) (stress-test), and self-efficacy levels (self-efficacy questionnaires). These measures will be collected and analyzed throughout the course of the intervention (3 months).