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NCT ID: NCT05012904 Completed - Pain Clinical Trials

Using Parental Involvement During Venipuncture to Reduce Venipuncture Pain and Anxiety in Children With Cancer

Start date: June 1, 2021
Phase: N/A
Study type: Interventional

This study aims to determine whether parental involvement during venipuncture reduces venipuncture pain and anxiety in children with cancer.

NCT ID: NCT04983290 Not yet recruiting - Parkinson Disease Clinical Trials

Outcomes to the Nutritional Need of Patients With Parkinson's Disease

W-Domus
Start date: November 1, 2021
Phase: N/A
Study type: Interventional

The intervention involves the identification of 140 patients (70 per group), fed throughout the duration of the study with the two different solutions indicated. The subject will be interviewed by identified and trained personnel in order to collect the information and data required by the study with frequency indicated for the individual evaluation sheets. The subject himself will be provided with all the contact and availability information of the referents of the firm for the purpose of requesting information or reporting events. The subject in the studio will be contacted weekly in order to evaluate the trend by the study referents, according to his availability, and personally interviewed by staff belonging to the research group.

NCT ID: NCT04895813 Completed - Colonoscopy Clinical Trials

The Effect of Education and Telephone Guidance at Colonoscopy

Start date: July 1, 2022
Phase: N/A
Study type: Interventional

Colonoscopy is an endoscopic procedure for diagnosing colon diseases. Patients should be prepared 2-5 days in advance for this procedure and intestinal cleansing should be provided. This is a difficult process and does not admit mistakes. The adequacy of the patient's pre-preparation for this process increases the chances of success. For preliminary preparation, it is recommended to train the patient and reinforce the trainings by phone. Education given to the patient; It contributes positively to patient outcomes, the workload of healthcare personnel in the institution, and costs. Therefore, this study has been planned.

NCT ID: NCT04778995 Completed - Education Clinical Trials

Online Training Program Model for Effective Management of Nursing Services in Times of Crisis Such as Pandemic

Start date: July 1, 2020
Phase: N/A
Study type: Interventional

This project is designed to determine the experiences of nurses working in healthcare organizations in the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pandemic and their approaches to problems experienced in qualitative design and from these results, a web-based education model is prepared for the effective management of nursing services, to increase the knowledge and skills of manager nurses. It was carried out in a quasi-experimental design. In the qualitative phase of the study, 28 people nurses were included (14 manager nurses and 14 nurses), and 61 nurse managers, including 30 intervention and 31 control group, participated in the randomized controlled quasi-experimental quantitative phase. Qualitative data were analyzed using the "Interview Form" through an in-depth interview method; Experimental data were collected via a pre- and post-questionnaire from nine web-based training videos. Qualitative data were analyzed in the MAXQDA 2020 program, and experimental data were analyzed in the Statistical Package for the Social Sciences (SPSS) 21.0 package program. Findings obtained from the qualitative stage; The problems regarding the institution's general management, the problems and approaches experienced by the nurses, and the problems and approaches experienced by the manager nurses were evaluated under three main themes. A pre-test / post-test questionnaire was applied to the intervention and control groups created due to the analysis of qualitative data.

NCT ID: NCT04730141 Completed - Nursing Clinical Trials

Effect of Mobilization Protocol on Mobilization

Start date: May 29, 2019
Phase: N/A
Study type: Interventional

The aim of this study is to determine the effect of early mobilization protocol on patients' mobilization status and patient care outcomes in patients who undergo major abdominal surgery. This study is a prospective non-randomized controlled clinical trial.

NCT ID: NCT04608929 Completed - Clinical trials for Urinary Incontinence

Kegel Exercise-focused Interventions in Elderly Women

Start date: December 21, 2017
Phase: N/A
Study type: Interventional

Purpose: This study was conducted to investigate the effects of Kegel exercises-focused intervention undergone by elderly women diagnosed with urinary incontinence on their incontinence, quality of life and perceived impact level. Design: The study has a single-blind randomized controlled experimental research design. Methods: The study was carried out between December 2017 and March 2019 with 60 elderly women registered at the Home Health Unit of a Metropolitan Municipality in Turkey. The women were assigned to the intervention (n=30) and control (n=30) groups. The participants in the intervention group were paid home visits to provide them with individual training and counseling on Kegel exercises. Whether the participants did the exercises was followed up by weekly phone calls. The frequency of urinary incontinence, the amount of urine leaking and the quality of life of the participants and their complaints about incontinence were assessed with the International Consultation on Incontinence Questionnaire Short Form and questions on the assessment of the perceived impact at the onset of the study (0th week), and at home visits paid at the 6th and 12th weeks after the intervention.

NCT ID: NCT04596137 Completed - Pain Clinical Trials

Kangaroo Care Reduces Infant Pain Caused By Vaccination

Start date: June 1, 2016
Phase: N/A
Study type: Interventional

The aim of this randomized controlled study determine the effect of KMC on pain in infants during vaccination.

NCT ID: NCT04593602 Withdrawn - Older Adults Clinical Trials

Early Mobilization in Older Adults With Acute Cardiovascular Disease

EM-HEART
Start date: April 1, 2023
Phase: Phase 3
Study type: Interventional

The EM-HEART study is a prospective, multi-centre stepped wedge cluster randomized trial to evaluate the effectiveness of a pragmatic early mobilization (EM) program to improve patient-centred and clinical outcomes in older adults with acute CV disease. There will be 256 participants ≥60 years old with acute CV disease enrolled at 6 participating Canadian hospitals. The study will investigate whether EM improves functional status during admission, as compared to usual care, and whether this leads to improved health-related quality of life post-hospitalization. Functional status will be measured with the validated Level of Function Mobility Scale. The primary outcome will be the Short-Form SF-36 physical component scale score at 1-month post-hospitalization. Secondary outcomes include functional status and hospital readmission at 1-month post-hospitalization.

NCT ID: NCT04582422 Completed - Nursing Clinical Trials

Interventional Touch Therapy in the Treatment of Children's Dental Clinics

Start date: May 20, 2020
Phase: N/A
Study type: Interventional

This study mainly wants to discuss the anxiety and fear of children's dental visits. For preschool children, separation anxiety can be obvious at this time. The main research is 1. To explore the degree of fear of dental visits in preschool children;2. Children who are touched therapy, there differences in fear of children 's dental treatment? If parents or important others can provide touching care to increase children 's sense of safety, reduce children 's fear of dental visits, and improve the quality of dental care The main purpose of the study.

NCT ID: NCT04421599 Active, not recruiting - Nursing Clinical Trials

Necessity of Aspiration in the Ventrogluteal Site

Start date: January 14, 2019
Phase: N/A
Study type: Interventional

H1: Aspiration is not necessary for IM injections applied from the ventrogluteal region. H2: Aspiration procedure increases pain in IM injections applied from ventrogluteal region. H3: The duration of the aspiration procedure on IM injections applied from the ventrogluteal region is effective on pain.