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NCT ID: NCT05210010 Enrolling by invitation - Clinical trials for Transthyretin Amyloid Cardiomyopathy (ATTR-CM)

A Prospective Study to Assess the Utility of CA-4F in a Canadian Cardiology Setting

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

This study will assess whether CA-4F can improve diagnosis of ATTR-CM in a community cardiology setting when used to screen electronic medical record data for patients suitable for follow-up investigations.

NCT ID: NCT05209373 Enrolling by invitation - Clinical trials for Cardiovascular Diseases

Optimizing a Self-compassion Intervention Designed to Improve Physical Activity Among Women at Risk for Heart Disease

Start date: January 9, 2022
Phase: N/A
Study type: Interventional

The investigators aim to optimize an intervention which teaches women at risk for cardiovascular disease (CVD) to cope with this risk using self-compassion (an attitude of kindness towards oneself) in order to adopt a physically active lifestyle. The investigators previously conducted a one-on-one self-compassion intervention for 11 women with CVD risk that successfully increased physical activity. However, meeting one-on-one with each participant was time and resource intensive. The primary purpose of the present study is to determine if group self-compassion intervention delivery is comparably effective to one-on-one delivery for increasing physical activity among women at risk for CVD. The investigators hypothesize that group delivery should be at least as effective as individual delivery at increasing physical activity. Furthermore, only women low in self-compassion were included in the previous study. The secondary purpose of the present study is to determine if women higher in self-compassion can also benefit from the intervention. The investigators hypothesize that participants at all levels of self-compassion should benefit similarly from the intervention. Finally, the tertiary purpose is to determine if delivery mode and self-compassion interact such that one method of delivery (group or one-on-one) is better suited to women at low, moderate, or high self-compassion. This outcome is exploratory only and the researchers present no hypothesis. The present study follows the methods of a randomized optimization trial. Women at risk for CVD will be randomly assigned to receive four sessions of combined physical activity behaviour change and self-compassion training in groups of six to nine or through one-on-one delivery. The intervention will provide one session to discuss participants' CVD risk and physical activity goals, and then three sessions of self-compassion training. Outcome measures will be assessed pre- and post-intervention. The effectiveness of the one-on-one and group conditions for improving the study outcomes will be examined. The present research will determine how best to deliver an intervention which teaches women to cope with their CVD risk using self-compassion in order to become more physically active. The results of the present study will inform an eventual efficacy trial.

NCT ID: NCT05196230 Enrolling by invitation - Clinical trials for Autism Spectrum Disorder

A Virtual Dental Office Experience for Children With Autism Spectrum Disorder

Start date: June 30, 2021
Phase: N/A
Study type: Interventional

The objective of this study is to evaluate the effectiveness of virtual reality (360° video) compared to a social story for reducing pre-visit dental anxiety for children with autism spectrum disorder (ASD) improve the dental visit experience for children, their families, and clinicians. The secondary objective is to perform a cost comparison analysis of the 360° video product as compared to a social story for Holland Bloorview's dental clinic.

NCT ID: NCT05195944 Enrolling by invitation - Diabetes Mellitus Clinical Trials

Semaglutide vs Sitagliptin

Start date: October 26, 2022
Phase: Phase 4
Study type: Interventional

The effect of once daily dosing of oral Semaglutide versus once daily dosing Sitagliptin on glycemic control, body weight, and safety and tolerability will be compared in Liver Transplant Recipients with poorly-controlled Diabetes Mellitus.

NCT ID: NCT05195788 Enrolling by invitation - Clinical trials for Congenital Heart Disease

Cardiac Rehabilitation in Congenital Heart Disease: Effects on Brain and Cognitive Functions

CongeNIRS
Start date: February 7, 2022
Phase: N/A
Study type: Interventional

The proposed trial is designed to evaluate the effect of an individualised cardiac rehabilitation program, consisting of aerobic and muscle strengthening exercises, on brain activity and cognitive functions in adults with congenital heart disease

NCT ID: NCT05181670 Enrolling by invitation - Clinical trials for SARS-CoV-2 Infection

The Canadian Respiratory Research Network Long COVID-19 Study

Start date: August 1, 2022
Phase:
Study type: Observational

Preliminary studies suggest that COVID-19 causes long-term lung damage, even in young, otherwise healthy people who did not need to go to hospital or the ICU. We seek to know how common long-term lung damage after COVID-19 is, who is most affected by it and what the effects of this damage are on other important aspects of people's lives. We plan to study a large sample of people with a history of COVID-19 infection from across Canada-some who needed hospitalization but most who did not. Through online questionnaires, we will determine their respiratory symptoms, quality of life and medical history. Then we will invite them to one of our thirteen Canadian testing centres to have special, thorough breathing tests. We hypothesize that COVID-19 leaves a significant proportion of people with measurable respiratory impairment. The information we learn about the effect of COVID-19 on the lungs will help patients and health care providers manage it better. It will also reveal how different COVID-19 variants affect the lungs. We will use this new knowledge to write a formal guide on what respiratory monitoring and testing should be done after COVID-19 infection. This will ensure that people affected by COVID-19 get the care they need to maintain their lung health.

NCT ID: NCT05174338 Enrolling by invitation - Clinical trials for Amyloidosis, Immunoglobulin Light-chain

Cardiac Amyloidosis Registry Study

CARS
Start date: January 8, 2020
Phase:
Study type: Observational

This registry is a observational, multi-center study designed to collect data and analyze it retrospectively on patients with cardiac amyloidosis who have been evaluated and treated at major amyloid centers across the US and internationally between 1997 and 2025.

NCT ID: NCT05145010 Enrolling by invitation - Achondroplasia Clinical Trials

Extension Study of Infigratinib in Children With Achondroplasia (ACH)

Start date: December 6, 2021
Phase: Phase 2
Study type: Interventional

This is a Phase 2, multicenter, open-label, extension (OLE) study to evaluate the long-term safety, tolerability, and efficacy of infigratinib, an FGFR 1-3-selective tyrosine kinase inhibitor, in subjects with ACH who previously completed a QED-sponsored interventional study, and potentially in additional subjects who are naïve to infigratinib treatment. Quality of Life assessments for this subject population will also be evaluated. Treatment-naïve subjects must have at least a 6-month period of growth assessment in the PROPEL study (Protocol QBGJ398 001) and will be enrolled in this OLE study only after a dose to be explored further is identified in Phase 2 Study QBGJ398-201.

NCT ID: NCT05125835 Enrolling by invitation - Clinical trials for Periodontal Diseases

Periodontal Maintenance and the COVID-19 Pandemic

Start date: November 21, 2021
Phase:
Study type: Observational

Periodontal disease is a chronic condition affecting the teeth and surrounding support structures, characterized by tooth loss and alveolar bone loss. Sanative therapy (ST) is the gold standard non-surgical treatment for periodontal disease and involves mechanically removing the subgingival bacteria from the periodontal pockets. Regular periodontal maintenance appointments are needed to maintain periodontal health after ST. Moreover, the periodontal health of individuals not requiring ST is also dependent on regular hygiene appointments. Due to Ontario's March 2020 COVID-19-related clinic closure for approximately 3 months along with a reduced numbers of appointments available due to guidelines of professional bodies and public health beyond this period of time, many appointments were considerably delayed or cancelled. The effects of this disruption to periodontal health in male and female patients who have undergone ST and continue with maintenance appointments or who attend for regular hygiene appointments have not yet been investigated.

NCT ID: NCT05116137 Enrolling by invitation - Brain Cancer Clinical Trials

The Impact of Resistance ExerciSe on Muscle Mass in GlioblaSToma Survivors

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

Glioblastoma patients are confronted with a debilitating disease associated with a low survival rate and poor quality of life. The goal of this study will be to reach a largely underrepresented population in the exercise literature and explore the role of a tailored circuit-based resistance training program on functional fitness (i.e., ability to carry out tasks of daily living) and associated health outcomes (e.g., quality of life) for GBM patients on active treatment.