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NCT ID: NCT04515758 Completed - Obesity Clinical Trials

Determining the Feasibility of Implementing a Combined Cognitive and Exercise Training Program for Older Adults in a Community Setting.

Start date: April 1, 2019
Phase: N/A
Study type: Interventional

The overarching aim of this project is to implement and evaluate a proven cognitive training regimen in combination with a community exercise program among older adults who attend wellness exercise programs at the YMCA. To support this aim, the investigators have developed a collaboration with the YMCA of Kitchener-Waterloo, which offer exercise programs targeted to older adults. The specific objectives are: (1) to evaluate the feasibility of a combined exercise and cognitive training in a community-setting among older adults; and (2) to conduct a preliminary evaluation and comparison of changes in cognitive function, physical function, well-being and self-efficacy with 12-weeks of combined exercise and cognitive training versus exercise alone. The hypothesis for each objective are as follows: (1) It is anticipated that this program will be feasible to implement and will be well accepted by the participants and exercise providers. (2) The investigators may not have the power to find statistically significant differences between the control and experimental groups for physical and cognitive function. However, the investigators expect to observe positive changes between the pre- and post-assessments, suggesting improved cognitive function and mobility as a result of the 12-week program.

NCT ID: NCT04521556 Completed - Quality of Life Clinical Trials

Effect of Epidural Anesthesia and Analgesia on Quality of Recovery After Unilateral Nephrectomy.

QoR
Start date: April 1, 2019
Phase: Phase 4
Study type: Interventional

Different modality of anesthesia and analgesia could influence a postoperative quality of recovery (QoR). This study is exploring early QoR after unilateral nephrectomy in the two groups of anesthesia. The first group had a light general anesthesia with thoracic epidural anesthesia and postoperative epidural analgesia with morphine and ropivacaine. The second group had general anesthesia and a continuous postoperative analgesia with tramadol. The postoperative QoR was evaluated 24 hours after surgery.

NCT ID: NCT04529824 Completed - Diabetes Clinical Trials

Glucose Risk Assessment in Employer Populations

Start date: April 1, 2019
Phase:
Study type: Observational

This is an observational study to understand the glucose characteristics of the general population (normal glucose, pre-diabetes, and diabetes). Glucose risk will be measured with laboratory HbA1c and continuous glucose monitor (CGM) derived metrics. Physical activity will also be measured using a Fitbit activity tracker. The study will inform future programs that use CGM and activity tracking to identify people at risk for diabetes in the population.

NCT ID: NCT04536818 Completed - Clinical trials for Penetrating Abdominal Trauma

Outcomes After Laparotomy for Penetrating Abdominal Trauma

Start date: April 1, 2019
Phase:
Study type: Observational

The purpose of this study is to evaluate outcomes of adult patients hospitalised due to penetrating abdominal trauma at a tertiary trauma hospital in South Africa. Our primary objective is to study the association between waiting time to surgery and outcome (mortality, complications, and length of hospital stay) in normotensive patients treated with laparotomy for penetrating abdominal trauma.

NCT ID: NCT04556708 Completed - Clinical trials for Periodontal Diseases

Ozonated Water Irrigation as an Adjunct to Periodontal Therapy

Start date: April 1, 2019
Phase: N/A
Study type: Interventional

The use of chlorhexidine or ozonized water in periodontal pockets accompanying NPT can provide a significant improvement in probing pocket depths compared to conventional treatment. However, the effect of subgingival ozonized water applications on VEGF and IGF levels, which are thought to play a role in the pathogenesis of periodontal disease and periodontal regeneration, should be examined.

NCT ID: NCT04557332 Completed - HIV-1-infection Clinical Trials

mHealth for ART Adherence by HIV+ African Americans

Start date: April 1, 2019
Phase: Phase 2
Study type: Interventional

The objective of this grant is to create and test a mobile app to support ART adherence among HIV+ African American adults.

NCT ID: NCT04568577 Completed - Ankle Sprains Clinical Trials

Effects of the Elastic Taping on the Chronic Ankle Instability

Start date: April 1, 2019
Phase: N/A
Study type: Interventional

This study will analyze the effects of an elastic taping application protocol in individuals with chronic ankle instability. One group will perform a protocol with increased tape tension for five weeks while the other group will receive the same tape without tension during the same period.

NCT ID: NCT04570605 Completed - Overactive Bladder Clinical Trials

Feasibility of Parasacral Transcutaneous Electrical Nerve Stimulation PTENS for Voiding Dysfunction in Peds Population

Start date: April 1, 2019
Phase: N/A
Study type: Interventional

Pilot study for determining feasibility of home parasacral transcutaneous electrical nerve stimulation in treatment of urinary urgency and incontinence.

NCT ID: NCT04571281 Completed - Clinical trials for Out-Of-Hospital Cardiac Arrest

Dynamics of the Capillary Lactate Levels in OHCA

Start date: April 1, 2019
Phase:
Study type: Observational

Serial capillary lactate measurements during cardiopulmonary resuscitation (CPR) in patients with out-of-hospital cardiac arrest (OHCA).

NCT ID: NCT04576884 Completed - Cataract Clinical Trials

Age-Related Changes and Cycloplegia-Induced Differences in the Human Crystalline Lens

Start date: April 1, 2019
Phase:
Study type: Observational

The ocular biometric parameters of the human crystalline lens including anterior chamber depth (ACD), lens thickness (LT), radii of curvature of anterior and posterior lens (ALR and PLR), lens equatorial diameter (LED), and lens vault (LV), automatically quantified by the CASIA2 (SS-OCT; Tomey, Nagoya, Japan). Images of iridocorneal angle were obtained using CASIA2 and the Schlemm' s canal (SC) and trabecular meshwork (TM) were quantified manually. Both cycloplegia and non-cycloplegia images were obtained.