Virtual Clinic

2

Review clinical trials related to Virtual Clinic. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Virtual Ward for Early Discharge in Patients Receiving Inpatient Care

This study evaluates the feasibility of providing hospital-level care at home for eligible patients through a Virtual Ward. Patients are discharged early from the hospital and monitored remotely using digital vital sign monitoring and anamnesis questionnaires. The primary aim is to determine if at least 30% of eligible patients can be safely and successfully transferred to the Virtual Ward under current Dutch healthcare conditions.

Participants needed: 306
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Erasmus Medical CenterUpdated: Feb 17, 2026Locations: 1
Eligibility criteria

Adult patients (≥18 years old). [+6]

Patients requiring continuous hospital-based monitoring or interventions that ca... [+6]

Status: Recruiting

Canada-wide Implementation of a Virtual Sexual Health and Rehabilitation eClinic (SHAReClinic) for Prostate Cancer Patients and Their Partners

The goal of this observational study is to evaluate the effectiveness of SHAReClinic, a national, virtual Sexual Health and Rehabilitation eClinic designed to support prostate cancer patients and their partners. Specifically, this study aims to assess SHAReClinic's impact on improving sexual function, satisfaction, and relational intimacy after treatment. The primary objective is to evaluate SHAReClinic's effectiveness across participating sites and determine its role in supporting long-term sexual health and well-being. As part of usual care, newly enrolled SHAReClinic patients will receive guided education modules and access to sexual health counselling at key recovery milestones. SHAReClinic seeks to expand access to sexual health care for prostate cancer patients across Canada by providing evidence-based, virtual sexual rehabilitation. Findings from this study will inform best practices in survivorship care and contribute to the development of a national standard for oncology sexual health interventions.

Participants needed: 575
Trial details
Age: 18+Biological sex: MaleType: ObservationalSponsor: University Health Network, TorontoUpdated: Dec 11, 2025Locations: 10Duration: 12 Months
Eligibility criteria

Patients who are scheduled for first-line treatment for localized prostate cance... [+5]

Patients on ADT alone as primary treatment, and/or patients on chemotherapy [+4]