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NCT ID: NCT04707937 Enrolling by invitation - Gynecologic Cancer Clinical Trials

Evaluation of a Brachytherapy Discharge Education Program to Improve Patient Care

BrachDEP
Start date: August 19, 2020
Phase: N/A
Study type: Interventional

Although brachytherapy is an effective treatment modality for gynecological cancer, a significant proportion of patients develop late treatment-related vaginal toxicity, negatively impacting their quality of life and limiting recurrent disease detection by preventing adequate clinical examination during the post-treatment surveillance period. Consistent with the literature, results from a study at Princess Margaret revealed that current vaginal toxicity management education and training may be inadequate. The investigators seek to implement and evaluate a new online brachytherapy discharge education program (BrachDEP) to support patient engagement in self-management.

NCT ID: NCT04707092 Enrolling by invitation - Clinical trials for Surgical Site Infection

Use of Preoperative and Postoperative Antimicrobial Treatment

Start date: June 1, 2021
Phase: Phase 4
Study type: Interventional

In this study, patients undergoing ear surgery (cochlear implantation, stapedotomy, tympanoplasty) will be randomized to one of two antibiotic treatment groups. One group will receive a single treatment with an antibiotic at induction The other group will receive the single intravenous treatment, plus a one week course or oral antibiotic

NCT ID: NCT04675229 Enrolling by invitation - Dementia Clinical Trials

Extending the Validation of SCREEN to Persons Living With Dementia or in Retirement Homes

SCREEN
Start date: September 25, 2022
Phase:
Study type: Observational

Older adults (≥ 55 years) who do not eat enough nutritious food are at risk of malnutrition. Malnutrition can lead to frailty, hospitalization, poor quality of life, and death. SCREEN (Seniors in the Community Risk Evaluation for Eating and Nutrition) is the leading nutrition risk screening tool for cognitively well older adults living in the community. The purpose of this study is to determine if SCREEN can be used to find nutrition risk among older adults diagnosed with mild cognitive impairment or dementia (i.e., MCI-D) living in the community and persons living in retirement homes. SCREEN and other nutrition and health measures will be completed in 600 older adults (300 living in retirement homes with or without MCI-D, and 300 living with MCI-D in the community). SCREEN will be completed twice to determine reliability, and persons with MCI-D will have their results compared to those of a caregiver who completes it on their behalf. A dietitian's assessment and rating of nutrition risk will be used as the gold-standard to determine validity.

NCT ID: NCT04673565 Enrolling by invitation - Hearing Loss Clinical Trials

Motivational Interviewing in Hearing Aid Users

MI-HAT
Start date: March 16, 2021
Phase: N/A
Study type: Interventional

Hearing loss is one of the most common chronic disabilities in the older adult population and affects their quality of life. Hearing aid use can improve one's quality of life by increasing a person's ability to detect, differentiate and locate sound, and improve speech recognition. Several factors seem to reduce motivation to use a hearing aid. Fears of exclusion and shame due to hearing loss are major deterrents to hearing aid use. Motivational interviewing (MI) is a counselling style aimed at creating desire in patients to change their behavior. There have been pilot studies that suggest one-on-one MI can increase hearing aid use, but other pilot studies found the reverse hence the evidence is inconclusive. The effectiveness of group MI therapy is also being investigated in MI research. While results in group MI research are promising, studies investigating group MI have been limited to substance abuse.

NCT ID: NCT04660006 Enrolling by invitation - Cataract Clinical Trials

Diabetic Retinopathy and OCT-A Changes Post-cataract Surgery

Start date: May 27, 2019
Phase:
Study type: Observational

The purpose of this study is to use optical coherence tomography angiography (OCT-A) to compare retinal vasculature after uncomplicated cataract surgery in patients with and without diabetic retinopathy.

NCT ID: NCT04641663 Enrolling by invitation - Aging Clinical Trials

Multi-target Dietary Supplement Tolerability in an Aging Population (MTDSST)

MTDSST
Start date: September 3, 2021
Phase: N/A
Study type: Interventional

This study is being performed to determine if a multi-ingredient dietary supplement is safe and easy to take by healthy older adults. Participants will be required to take one of three different doses of the dietary supplement for 90 consecutive days and complete wellness surveys and a daily log while taking the supplement. Participants will also provide blood samples at the start of the study, after 30 days, and at the end of the study which will help determine how participants respond to the supplement.

NCT ID: NCT04635540 Enrolling by invitation - Parkinson Disease Clinical Trials

Decreased Empathy and Emotion Recognition in Patients With Neurodegenerative Disease

Empathy
Start date: July 22, 2019
Phase: N/A
Study type: Interventional

This study evaluates an educational brochure tailored to caregivers of people with Alzheimer's disease, Parkinson's disease dementia, Lewy body disease, frontotemporal dementia, and vascular disease dementia. The goal of the brochure is educating caregivers about the decreased ability to detect emotion and decreased empathy that can be seen in dementia, increasing caregiver competence in providing care, and teaching caregivers ways to manage over time that lessens burden and improves quality of life.

NCT ID: NCT04602832 Enrolling by invitation - Well-Being Clinical Trials

Enduring Happiness and Continued Self-Enhancement (ENHANCE) for COVID-19

EN-COVID-19
Start date: October 14, 2020
Phase: N/A
Study type: Interventional

This study is a randomized controlled trial of an online, evidenced-based intervention (the ENHANCE program) that was modified to address the health and well-being challenges of COVID-19. Eligible participants will be randomized into the ENHANCE or Wait-List Control group over a 12-week period. ENHANCE participants will be introduced, and asked to practice, 10 evidenced-based principles and skills of happiness and well-being. Participants will complete an online survey about their health and well-being at baseline, midway (or 6 weeks), post-assessment (or at the end of the 12-week study), and 3-months following the end of the study.

NCT ID: NCT04588415 Enrolling by invitation - Bereavement Clinical Trials

Supporting Family Members With Severe Grief Reaction During the COVID-19 Pandemic

Start date: January 3, 2021
Phase: N/A
Study type: Interventional

This is a feasibility study taking place at The Ottawa Hospital (TOH), Hôpital Montfort, and Queensway Carleton Hospital that seeks to evaluate the impact of the COVID-19 pandemic on family member bereavement and study the effect of virtual support groups on reducing risk of developing Severe Grief Reaction (SGR). This project is inviting family members of deceased patients at either of the three before mentioned sites to enroll in this study.

NCT ID: NCT04568928 Enrolling by invitation - Clinical trials for Incomplete Spinal Cord Injury

Powered Exoskeleton Combined With Functional Electrical Stimulation in Clinical Practice

Start date: December 10, 2020
Phase: N/A
Study type: Interventional

After partial spinal cord injury, gait deficits may be present and often remain even after intensive rehabilitation. New robotic technologies have recently emerged to help augment the extent of rehabilitation. However, these are complex tools to integrate into clinical practice and little is known about the potential factors that may influence the uptake of a locomotor program using this technology by clinicians. The goal of this project is to bring together researchers, administrators, clinicians and patients to define and implement an overground robotized gait training program in clinic. We will also investigate the added value of leg and trunk muscle stimulation combined with robotic walking training, to see if it could enhance recovery.