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Medication Adherence clinical trials

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NCT ID: NCT02676128 Completed - HIV Clinical Trials

Mobile Health Application to Improve HIV Medication Adherence

Start date: March 2016
Phase: N/A
Study type: Interventional

Inadequate adherence to antiretroviral therapy (ART) can impede successful viral suppression and consequently lead to negative health consequences. This study aims to refine and test the efficacy of a mobile health ART adherence application (ARTAA), delivered over a smartphone, with helping individuals improve their ART adherence.

NCT ID: NCT02624193 Completed - HIV Clinical Trials

Health Improvement for Baltimore Youth

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

Preliminary data from the investigators' National Center for Complementary and Alternative Medicine (NCCAM)-funded R21 on mindfulness-based stress reduction (MBSR) in HIV-infected youth suggest an association between mindfulness and improved self-regulation and medication adherence. This randomized, controlled trial will help the investigators to better understand the specific impact of MBSR on HIV medication and treatment adherence in HIV-infected youth, and the efficacy of MBSR in the amelioration of stress and improved self-regulation.

NCT ID: NCT02604901 Completed - Clinical trials for Medication Adherence

Effect of Community Pharmacist Intervention on Adherence to Long-Term Medications

ECO-PHIL
Start date: June 2012
Phase: N/A
Study type: Interventional

The 4-arm factorial design RCT tested the impact of a behavioral intervention (SBI or BI), a reminder device (Pillbox), and the combination of the two on adherence in adult patients who filled a prescription for oral medications to treat diabetes or hyperlipidemia.

NCT ID: NCT02603536 Completed - HIV Clinical Trials

WelTelOAKTREE: Text Messaging to Support Patients With HIV/AIDS in British Columbia

WelTelOAKTREE
Start date: April 2013
Phase: N/A
Study type: Interventional

WelTel Oak Tree is a repeated measures study that enrolled 85 HIV+ individuals from the Oak Tree Clinic at BC Women's Hospital. Participants were be provided with a cell phone and/or unlimited text messaging capability if they do not have it already, and for one year received a weekly text message stating "How are you". Participant problems and non-responses were be followed up by a nurse. Data on demographics, CD4 counts, HIV viral loads, HIV medication adherence and attendance at appointments was collected for the year prior to the intervention and during the intervention for comparison. Data assessing quality of life was also collected at three points during the one year study period. Cost effectiveness and cost benefit of the intervention is being studied to assess feasibility of transferring the intervention to a programmatically funded facet of patient care.

NCT ID: NCT02543723 Completed - Clinical trials for Medication Adherence

Telehealth-based Strategies to Increase Oral Chemotherapeutic Agent Medication Adherence

Start date: November 15, 2015
Phase: N/A
Study type: Interventional

Oral chemotherapeutic agents (OCAs) are increasingly being used as an alternative to traditional intravenous chemotherapy, and factors promoting this trend include increased survival times requiring long-term therapy, acceptability among patients, convenience, and cost savings due to reduced hospital time. Although OCAs are commonly preferred by patients, adherence to these medications vary. Suboptimal medication adherence leads to loss of treatment efficacy, increased toxicity, and increased health care costs. Thus, it is critical to develop and test interventions that effectively improve adherence to OCAs. Although the medication adherence literature has been criticized for methodological issues, some components of interventions have had promising results on adherence such as electronic monitored adherence feedback, cognitive-education, nurse-based interventions, and technology-based or telehealth strategies. The investigators propose to unify components of these effective approaches in a novel way to assess the efficacy and feasibility of two telehealth-based strategies (electronic medication-event monitoring with feedback and tailored nurse coaching which includes cognitive-education) in an effort increase OCA adherence among cancer patients who are at high-risk for non-adherence in rural eastern North Carolina.

NCT ID: NCT02524548 Completed - Breast Cancer Clinical Trials

SMS Reminders to Improve Medication Adherence of Aromatase Inhibitors

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

The purpose of this study is to determine whether weekly SMS reminders are effective in improving medication adherence of adjuvant aromatase inhibitors in women with breast cancer.

NCT ID: NCT02490423 Completed - Clinical trials for Medication Adherence

Improvement in Medication Adherence Through the Implementation of Personalized Nudges: the ENCOURAGE Trial

ENCOURAGE
Start date: March 2016
Phase: N/A
Study type: Interventional

This study will determine whether a complex, data-driven protocol for assessing patient needs and providing "nudges" (reminders to be adherent with medication prescriptions) improves adherence with cardiovascular medications. This will be accomplished by performing a 12-month clinical trial of patients with an indication for statin therapy. Participants will be randomized to either an intervention or standard-of-care arm and will be followed via passive electronic means to determine if they are adherent with medication prescriptions.

NCT ID: NCT02484521 Completed - Schizophrenia Clinical Trials

Prepulse Inhibition (PPI) of Startle Reflex in Schizophrenia Patients Related to Type of Treatment and Illness Duration

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

PPI is an objective measure to assess pre-attentive processes that have already been tested before in the case of schizophrenia. The investigators aim to assess through this instrument two main characteristics, that the investigators assume are of relevance which are the duration of illness and the type of pharmaceutical treatment, patients receive. The investigators believe these two main characteristics are critical to the ability of the patients in improvement of their PPI response to startle reflex.

NCT ID: NCT02419066 Completed - HIV Clinical Trials

Examining HIV Treatment Adherence During Early Disease

META
Start date: February 2015
Phase:
Study type: Observational

Determine the level, patterns, and correlates of objectively measured ART adherence in early and advanced-stage disease, among pregnant and non-pregnant individuals, to determine the need and nature of interventions to support early ART adherence in Uganda and South Africa

NCT ID: NCT02390908 Completed - HIV Clinical Trials

Improving HIV and Alcohol-Related Outcomes Among HIV+ Persons in Clinic Settings

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

Alcohol use is increasingly recognized as a key factor in morbidity and mortality among HIV-positive individuals and represents an important public health concern, given its associations with medication non-adherence, increases in viral load, poor immunologic outcomes (lower cluster of differentiation 4, or CD4, counts), drug resistance, lower health care utilization, comorbidities (HIV/viral hepatitis coinfection), and poor health outcomes overall. Adherence to HIV medications has a double public health benefit, both in terms of slowing disease progression and improving health outcomes among HIV-positive individuals and in helping to curb the sexual transmission of HIV. The objective of this study is to implement a multisite comparative effectiveness trial in real-world clinical settings with three intensities of treatment to test the clinical and cost effectiveness of an efficacious, theory-based behavioral intervention (PLUS) in improving adherence to antiretroviral therapy (ART) and alcohol-related outcomes among HIV-positive individuals who drink alcohol at harmful or hazardous levels. The study is being conducted in collaboration between the Center for HIV Educational Studies and Training (CHEST) at Hunter College at the City University of New York (CUNY) and the Spencer Cox Center for Health at the Institute for Advanced Medicine, Mount Sinai Health System.