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Patient Compliance clinical trials

View clinical trials related to Patient Compliance.

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NCT ID: NCT05297188 Completed - Sleep Clinical Trials

The Effect of Ergonomic Sleep Mask Usage on Patients' Sleep Quality and Comfort

Start date: September 1, 2020
Phase:
Study type: Observational

In intensive care units, the sleep quality of patients decreases considerably due to reasons such as alarm sounds of some special devices, the number of healthcare professionals working in comparison to other clinics, their circulation is high, and the lights are constantly on.Studies conducted in intensive care units to facilitate the transition of patients to sleep and to improve sleep quality;has revealed that non-pharmacological applications increase sleep time and quality, reduce sleep disturbance,delirium,post-traumatic stress disorder and duration of stay in the intensive care unit.Although wearing earplugs and eye masks is a cost-effective and safe method and can improve perceived sleep quality in patients,eye masks and ear plugs are sometimes not comfortable.While the ear plugs dislocate during night sleep may cause the patients to wake up again,there are also situations such as the eye masks not being sized properly for the patients' eyes,and the part of the mask surrounding the head is thin and tense, disturbing the patient.By eliminating this situation that disturbs the patients, other solutions are needed to increase the quality of sleep without being affected by intensive care light and noise. The project was planned to determine the effect of the ergonomic sleep mask on the sleep quality and comfort of patients in surgical patients whose treatment and care continues in intensive care units.The sample of the project consists of 128 patients by performing power analysis.Patients will be divided into two groups as 64 randomized patients in the control and experimental groups by applying block randomization.While there is no application to the experimental and control groups on the first night, an ergonomic sleep mask will be worn to the experimental group,and an ear plug and eye mask will be worn to the control group.At the end of the first night and the second night, the sleep quality of the patients will be evaluated with the 'Richard Campell Sleep Scale' and their comfort levels with the 'Visual Analogue Scale'.The data of the project will be collected using the Patient Information Form prepared in accordance with the literature. In the analysis of the data,Mann-Whitney U test, t test in independent groups, one-way ANOVA test and correlation analysis will be done.

NCT ID: NCT04656028 Recruiting - Clinical trials for Medication Adherence

Genetic Testing and Motivational Counseling for FH

GENMOTIV-FH
Start date: June 15, 2020
Phase: N/A
Study type: Interventional

To date, there are highly effective lipid-lowering drugs, the combination of which makes it possible to achieve the target level of LDL-C in most patients with familial hypercholesterolemia (FH). However, the effectiveness of treatment of FH patients strongly depends on adherence to lipid-lowering therapy and to the healthy lifestyle, as well as the detection of the disease and the therapy prescription as early as possible, better in childhood. The aim of the study is to assess the impact of genetic testing and motivational counseling on the effectiveness of treatment and cascade screening in patients with FH.

NCT ID: NCT04327856 Completed - Clinical trials for Patient Satisfaction

The Subjective Pre-, Intra-, and Postoperatively Experiences of Patients Undergoing Cataract Surgery.

Start date: February 15, 2020
Phase:
Study type: Observational

Assessment of types and intensity of unpleasant experiences pre-, intra-, and postoperatively in the patients undergoing cataract surgery, using especially designed questionnaire. Strategic aim: formulation of algorithm and modification of perioperative approach to patient qualified to undergo phacoemulsification procedure.

NCT ID: NCT04291807 Completed - Patient Compliance Clinical Trials

Video Assisted Education Before ERCP

Start date: September 1, 2017
Phase: N/A
Study type: Interventional

It was aimed to study the effect of video assisted education about endoscopic retrograde cholangiopancreaticography (ERCP) on anxiety levels of patients who planned to undergo ERCP for any reason.Video revealing the ERCP procedure was shown to the patients in one group and not shown to the other. Then anxiety levels and pain scores have been obtained before and after the procedure in both groups

NCT ID: NCT04249518 Not yet recruiting - Patient Compliance Clinical Trials

Video Extradition of Continuous Positive Airway Pressure - Influence on Compliance

Start date: May 15, 2020
Phase: N/A
Study type: Interventional

Confirming or denying it in the future is an opportunity for certain patient groups to have the option of video delivery. So that in calm circumstances and possibly. several times can review the video and equipment in the home and hopefully achieve the same or better compliance with the ongoing treatment.

NCT ID: NCT04243980 Not yet recruiting - Clinical trials for Patient Satisfaction

Anatomical Femoral Stem in Total Hip Arthroplasty

THR
Start date: February 1, 2020
Phase:
Study type: Observational

A study that detect the femoral anteversion after total hip arthroplasty using short anatomical femoral stem compared to the contrast side

NCT ID: NCT04169165 Not yet recruiting - Nephrolithiasis Clinical Trials

Patient Compliance for Metabolic Evaluation and Medical Management in Calcium Stone Patients

Start date: January 2020
Phase:
Study type: Observational [Patient Registry]

Calcium oxalate stone, the most common type worldwide, has a recurrence rate of around 50% in ten years. Therefore, identifying the underlying pathophysiological aspects via metabolic evaluation and suggestions for medical & dietary prophylaxis in calcium stone patients is of upmost importance. However, one of the greatest problem with metabolic evaluation and subsequent therapeutic advices is the patient compliance. Therefore, it is important to identify factors related to patient compliance for metabolic evaluation and medical & dietary prophylaxis in calcium stone patients

NCT ID: NCT04145245 Recruiting - Patient Compliance Clinical Trials

A Randomized Controlled Trial to Assess the Effect of L-carnitine in Patients With Diabetic Peripheral Neuropathy to Relief Pain and Symptom Improvement

Start date: April 17, 2018
Phase: Phase 2
Study type: Interventional

Diabetic Peripheral Neuropathy (DPN) is a common complication of diabetes mellitus. The prevalence rate is approaching towards a peak throughout the world including Bangladesh. The current intervention used in peripheral neuropathy does not bring satisfactory result. Recent trial shows that L-carnitine is effective and safe in DPN. So it is expected that L-carnitine may produce better effect in compared to other medicine used previously for alleviation of DPN.

NCT ID: NCT04104425 Completed - Patient Compliance Clinical Trials

Lactate Level and Gastrointestinal Bleeding

Start date: January 15, 2020
Phase:
Study type: Observational

Acute gastrointestinal bleeding is a common emergency with significant morbidity, mortality, and cost. Appropriate risk stratification of patients presenting with acute gastrointestinal bleeding aids in the triage of patients to determine need for hospital admission and the need for emergency endoscopic intervention. Increased blood lactate levels are common in critically ill patients. Our study will evaluate the usefulness of lactate measurements on resources utilisation ( intensive care unit admission, length of hospital stay) and other patient-oriented outcomes ( need for transfusion and endoscopy) in patients with acute gastrointestinal bleeding.

NCT ID: NCT04052750 Recruiting - Clinical trials for Functional Gastrointestinal Disorders

SMS Reminders and Treatment Compliance and Efficacy in Patients With FGIDs

Start date: April 30, 2019
Phase: N/A
Study type: Interventional

The effect of SMS follow-up on drug compliance and efficacy in patients with FGIDs has not been reported in the literature. We, therefore, conducted a prospective randomized controlled trial to investigate whether SMS follow-up could improve treatment adherence in patients with FGIDs, which in turn would help symptom relief and improve treatment outcomes.