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Adherence clinical trials

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NCT ID: NCT05237921 Completed - Clinical trials for Gastrointestinal Cancer

Adherence to Exercise and Dietary Intervention in Cancer Patients

CEDI
Start date: June 15, 2018
Phase: N/A
Study type: Interventional

Intervention programs in cancer patients have been proposed with the aim of improving outcome. Bearing in mind that compliance is a limiting factor to the benefit provided from exercise and diet, assessing adherence to these interventions is paramount before pursuing further studies. Therefore the purpose of this study was to study the adherence of gastrointestinal cancer patients to a Combined Exercise and Dietary Intervention (CEDI) during neo-adjuvant chemotherapy.

NCT ID: NCT04240132 Completed - Clinical trials for Microbial Colonization

Hand Hygiene Practices and Microbial Contamination on Feeding Tubes and Other Components of Feeding Systems

Start date: January 2, 2020
Phase: N/A
Study type: Interventional

Enteral feeding tube (EFT) and component of feeding systems can serve as a reservoir of microorganisms, and the main reason is inappropriate hand hygiene practices. The aim of the project is to determine colonization of microorganisms on the EFT and other components and assess the relation between colonization and adherence to hand hygiene practices by healthcare workers in the intensive care unit. This prospective, observational and semi-experimental study will be conducted in one year. The project will be completed with healthcare workers and 51 patients who are feeding enteral route via nasogastric tube at least for three days. The researchers will provide training to healthcare workers in accordance with the World Health Organization (WHO) Hand Hygiene Guidelines. Hand hygiene behaviors of the participants will be observed and the question forms will be filled before and after training by researchers. The samples for microbial analysis will be collected from the EFT by sterile swaps.

NCT ID: NCT04081441 Completed - Clinical trials for Mental Health Wellness 1

Impacts of Clean Cookstoves and Empowerment Training on Women's Health in Refugee Settings

Start date: August 1, 2018
Phase: N/A
Study type: Interventional

The main objective of this study is to understand the links and outcomes of adoption of a cleaner cookstove/fuel and exposure to a personal empowerment training on women's health outcomes in a Congolese refugee camp in Rwanda, with a focus on gender-based violence (GBV).

NCT ID: NCT02938533 Completed - HIV Infection Clinical Trials

Social Norms and Priming to Improve Adherence to Antiretroviral Therapy and Retention in Care

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

Interventions incorporating constructs from behavioral economics and psychology have the potential to enhance HIV 'treatment as prevention' (TasP) strategies. To test this hypothesis, the investigators evaluated a combination intervention to improve antiretroviral therapy (ART) adherence based on the concepts of social norms and priming.

NCT ID: NCT02915367 Completed - HIV/AIDS Clinical Trials

Monitoring Pre-exposure Prophylaxis for Young Adult Women

MPYA
Start date: December 21, 2016
Phase: N/A
Study type: Interventional

Next generation real-time monitoring for PrEP adherence in young Kenyan women

NCT ID: NCT02858713 Completed - Adherence Clinical Trials

Adherence in Topical Treatment of Psoriasis

Start date: January 9, 2017
Phase: Phase 4
Study type: Interventional

Medical adherence to topical corticosteroid products in psoriasis patients is a main determinant for poor treatment effect. The investigators aim to test if a multifaceted intervention delivered in an app (MyPso QualityCareTM owned by Leo Pharma) for smartphones combined with an Electronic Monitor (EM) (Teslo) can improve medical adherence among psoriasis patients treated with a topical calcipotriol/betamethasone dipropionate foam combination (Cal/BD) (Enstilar©). The study is classified as a phase 4 study, since it is studied if improved use of Enstilar© results in improved treatment outcomes. Link to published study protocol: https://bmcdermatol.biomedcentral.com/articles/10.1186/s12895-018-0071-3 Link to published results from the study: https://onlinelibrary.wiley.com/doi/abs/10.1111/bjd.16667

NCT ID: NCT02858050 Completed - Adherence Clinical Trials

Portal-724 MEMS for Medication Adherence Patients Taking HCV Medications

Start date: September 9, 2016
Phase:
Study type: Observational

The study will look at real-time adherence monitoring with Portal-724 MEMS cap. It integrates medication bottle, Smart Cap, Pill Dispenser, Embedded Computer, Embedded Cellular Modem and Tamper Proof apparatus. This device is capable of transmitting pill dispensing events from the patient's home to the Cloud over Cellular and IP networks. The transmission is done in real time if cellular coverage is above 1-bar, but if the cell signal is not available or if the signal is below the threshold, then the device Store-and-Forward feature is automatically activated. The patient will be randomized to real-time monitoring or to have monitoring data download monthly at each study visit while taking hepatitis C medications

NCT ID: NCT02820753 Completed - Adherence Clinical Trials

A Universal Medication Schedule to Promote Adherence to Complex Drug Regimens

Start date: April 3, 2017
Phase: N/A
Study type: Interventional

This study will leverage available technologies and test strategies to impart the Universal Medication Schedule (UMS) in primary care to help patients understand, consolidate, safely use, and adhere to their complex medication regimens.

NCT ID: NCT02736851 Completed - Adherence Clinical Trials

Telemedicine to Manage Chronic Neck Pain at Home

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

The aim of the study is to investigate if a home-based structured physician-directed, nurse-managed telemedicine program can increase adherence to a home exercise program and decrease neck pain and disability. The study is carried out in 100 consecutive patients with chronic non-specific neck pain. All patients referred to a rehabilitation Institute for an out-.patient visit complete a stretching exercise program and are instructed and encouraged to perform exercises regularly once at home. At the end of the rehabilitation, the patients are randomized into two groups of 50 patients each. Patients of the first Group are allocated to a home-based telemedicine (HBT), while those of the second group receive only the recommendation to continue exercising at home (Control group). The HBT intervention consists of fortnightly scheduled phone calls to patients over the 6-month course of the study. A nurse-tutor encourages the patient to perform regularly physical activity and prescribes exercises. Adherence to home exercises is evaluated 15 days and 6 months after the end of the outpatient rehabilitation, while pain intensity and neck disability are assessed and compared in the two groups at entry and 6 months after the end of the outpatient rehabilitation .

NCT ID: NCT02480530 Completed - Clinical trials for Coronary Artery Disease

Using Feedback Reports to Improve Medication Adherence

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

The purpose of this research study is to improve statin medication adherence among Veterans with coronary artery disease with poor adherence to medications. The investigators are testing if newer technology pill bottle devices linked with individual feedback and/or social incentive strategies can improve medication taking behavior.