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Chronic pain is one of the main factors influencing workers' retention at work. Considering that the prevalence of suffering from chronic pain increases with age, older workers are most likely to be absent from work because of their pain. Transcranial direct current stimulation (tDCS) is a treatment option to reduce chronic pain. This study aims to document the effect of tDCS on pain and work retention in older workers and to compare the traditional tDCS protocol (5 sessions) with an enhanced protocol (11 sessions).
Conditions:
Aging | Chronic PainLocation:
- Clinique régionale de la gestion de la douleur - CISSSAT, Rouyn-Noranda, Quebec, Canada
- Centre de Recherche sur le Vieillissement, Sherbrooke, Quebec, Canada
Sex:
ALLAges:
Over 56The purpose of the present study is to conduct a two-arm Randomized Control Trial (RCT) comparing individuals receiving the 90Second Caregiver health letter, with a usual care (routine care received by caregivers) control group. The goals of the present study are: * To evaluate the effectiveness of the 90Second Caregiver health letter in improving caregiver's self-efficacy (primary outcome), savouring, and quality of life (secondary outcomes). * To evaluate the effectiveness of the 90Second Caregiver health letter in reducing caregiver's psychological strain and caregiver burden (secondary outcomes). * To examine the impact of levels of engagement with the 90Second Caregiver health letter on primary and secondary outcomes. * To assess the usability of the 90Second Caregiver health letter, as it relates to the relevance of topic, user friendliness, and appropriateness of the readability levels. * To evaluate psychometric properties of self-constructed measures in 90Second newsletter.
Conditions:
Acquired Brain Injury | CaregiversLocation:
- IWK Health Centre, Halifax, Nova Scotia, Canada
Sex:
ALLAges:
Over 18The goal of this clinical trial is to evaluate the safety and effectiveness of cytisine as a smoking cessation treatment in individuals with concurrent alcohol use disorder.
Conditions:
Tobacco Use Disorder | Smoking Cessation | Alcohol Use DisorderLocation:
- Center for Addiction and Mental Health, Toronto, Ontario, Canada
Sex:
ALLAges:
18 - 65A multicentre, parallel group, randomized controlled Phase II clinical trial evaluating neoadjuvant Atezolizumab/Bevacizumab versus neoadjuvant SBRT in patients with biopsy proven solitary HCC with PVTT involving the portal vein branches. Both arms are considered experimental, and as such, a Simon two-stage design will be initially used within both arms. Only if both arms are deemed of interest for further study will a comparison between arms, using a pick-the-winner design, be conducted. Following the completion of neoadjuvant therapy, study participants will undergo a CT scan or MRI to assess tumour response to neoadjuvant therapy. Hepatic resection will be performed for those participants who meet the surgical resection criteria.
Conditions:
Hepatocellular Carcinoma | Portal Vein Tumour ThrombosisLocation:
- Ottawa Regional Cancer Centre, Ottawa, Ontario, Canada
- Juravinski Cancer Centre, Hamilton, Ontario, Canada
- McGill Cedars Cancer Centre, Montréal, Quebec, Canada
- Tom Baker Cancer Centre, Calgary, Alberta, Canada
- Princess Margaret Cancer Centre, Toronto, Ontario, Canada
- Cross Cancer Institute, Edmonton, Alberta, Canada
- 8. Centre the recherche du Centre hospitalier de l'Université de Montréal - CHUM, Montreal, Quebec, Canada
Sex:
ALLAges:
Over 18This is single centre pilot, randomized controlled trial assessing postpartum prophylactic anticoagulation with 3 weeks of LMWH followed by 3 weeks of Aspirin compared to standard of care of prophylactic LMWH for 6 weeks at moderate to high risk of developing VTE.
Conditions:
Venous ThromboembolismLocation:
- Mount Sinai Hospital, Toronto, Ontario, Canada
Sex:
FEMALEAges:
Over 18This pilot study initiates a research program testing the early technical and clinical performance of a novel procedure for MRI-guided high-dose-rate (HDR) prostate brachytherapy. Testing will proceed in two cohorts of patients. In Arm 1, patients with locally recurrent prostate cancer after radiotherapy will receive tumor-targeted salvage HDR brachytherapy. Arm 1 of the study will be coordinated and closely integrated with a separate concurrent study of MRI-guided prostate biopsy, which will be performed prior to accrual to Arm 1 of this trial (UHN 05-0641-C). In arm 2, patients with locally advanced prostate cancer will receive a boost of prostate-targeted HDR brachytherapy during external beam radiotherapy. This technique will be prospectively evaluated in up to 100 patients. Preliminary data acquired in this pilot study will determine the technical limits of MRI guided HDR brachytherapy and will be critical for the judicious conduct of a subsequent phase II clinical trial. This proposal is innovative in two fundamental ways: MRI-guidance, and specific tumor targeting for HDR brachytherapy. Successful completion of this study will further individualize local therapy, not only for the benefit of the proportion of cancer patients for whom initial radiotherapeutic interventions have failed, but also provide valuable technical and clinical validation that these novel image-guided (IG) approaches are clinically feasible and could be applied more broadly in prostate cancer therapy.
Conditions:
Patients With Prostate CancerLocation:
- University Health Network, Princess Margaret Hospital, Toronto, Ontario, Canada
Sex:
MALEAges:
Over 18Poorly controlled chronic pain in teens can impact quality of life, increase opioid use and is a risk factor for developing chronic pain in adulthood. Currently, there is a shortage of support to help teens manage chronic pain in the community and the support that did exist has been significantly scaled back due to the COVID-19 pandemic. This research study will investigate, based on questionnaires with teens and healthcare providers and interviews with teens, whether pain rehabilitation virtual reality is easy to use and understand, satisfactory to use, and whether it may improve pain, mobility, and function for the teens using the program compared to those doing standard physiotherapy treatment over videoconference.
Conditions:
Pain, ChronicLocation:
- Hospital for Sick Children, Toronto, Ontario, Canada
Sex:
ALLAges:
12 - 18Resistance exercise training (RET) in children and adolescents has become a popular area of research, with a growing body of evidence supporting its use. Position and consensus statements about RET for children indicate that it is safe and effective at increasing muscular strength, improving sport performance, and mitigating injury risk. Neural and muscular mechanisms can improve muscle strength following RET. Neural factors include improved recruitment and firing of an individual's motor units, and muscular factors primarily include an increase in the size of the muscle (hypertrophy). In children, little is known about how these mechanisms relate to muscle strength. There is very little evidence of morphological changes following RET in children. Therefore, conventional wisdom is that children rely only on neural factors to improve strength following RET. Nevertheless, some studies have suggested RET-induced muscle hypertrophy in children and adolescents, indicating that with certain training protocols, children may achieve muscle growth. Hypertrophy of muscle fibres occurs when the rate of muscle protein synthesis (MPS) is greater than the rate of protein breakdown, and is enhanced with the ingestion of dietary amino acids. Due to ethical concerns with obtaining muscle samples (i.e., from muscle biopsies) in pediatric populations, MPS rates have not been previously assessed following RET in children. Recent advancements in stable-isotope methodology (specifically, leucine) allow for the estimation of MPS in a non-invasive breath test. The objective of the proposed research is to examine the effects of an acute bout of RET on leucine retention (a proxy for MPS) in children, adolescents, and adults using a non-invasive breath test.
Conditions:
Exercise | Dietary SupplementationLocation:
- Brock University, St. Catharines, Ontario, Canada
Sex:
ALLAges:
7 - 35The objective of the study is to investigate the metabolism of cells in the ascites tumour microenvironment of ovarian cancer patients. This observational study involves intravenous infusion of \[U-13C\]glucose into patients during standard paracentesis.
Conditions:
Ovarian Cancer | AscitesLocation:
- Jennifer Rauw, Victoria, British Columbia, Canada
Sex:
FEMALEAges:
Over 18Intracranial bifurcation aneurysms are commonly repaired with surgical and with endovascular techniques. Wide-necked bifurcation aneurysms (WNBA) are a difficult subset of aneurysms to successfully repair endovascularly, and a number of treatment adjuncts have been designed. One particularly promising innovation is the WEB (Woven EndoBridge), which permits placement of an intra-saccular flow diverting mesh across the aneurysm neck, but which does not require anti-platelet agent therapy. Currently, which treatment option leads to the best outcome for patients with WNBA remains unknown. There is a need to offer treatment with the WEB within the context of a randomized care trial, to patients currently presenting with aneurysms thought to be suitable for the WEB.
Conditions:
Intracranial Aneurysm | Unruptured Cerebral Aneurysm | Cerebral Aneurysm | Brain Aneurysm | Ruptured Cerebral AneurysmLocation:
- Centre Hospitalier de l'Université de Montréal, Montréal, Quebec, Canada
- Hamilton Health Sciences - McMaster University, Hamilton, Ontario, Canada
- University of Alberta Hospital, Edmonton, Alberta, Canada
- University of Manitoba Hospital, Winnipeg, Manitoba, Canada