Clinical trials

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Search and review clinical trials. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Efficacy of Remote Monitoring in Patients Treated for Moderate to Severe Major Depressive Episodes

Mood disorders like depression and bipolar disorder are widespread and cause serious psychological, cognitive, and social impairments, with a high burden on healthcare systems. Edra PRO is a digital medical device developed to support clinical decision-making and remotely monitor symptoms in psychiatric patients. The EC-102 randomized controlled trial will evaluate its impact compared to usual care on symptoms, quality of life, healthcare costs, comorbidities, and user adherence and satisfaction.

Participants needed: 594
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: ResilienceUpdated: May 1, 2026Locations: 6
Eligibility criteria

Adults (≥18 years old) meeting ICD-11 criteria for a moderate to severe major de... [+1]

Pregnant women [+3]

Status: Recruiting

Randomized Controlled Trial of Remote Symptoms Monitoring With Resilience PRO Compared to Care As Usual Only

The goal of this clinical trial is to learn if Resilience PRO, a digital solution performing remote symptoms monitoring, can improve the quality of life of patients with a diagnosis of cancer receiving systemic anticancer treatment. The main question it aims to answer is: \- Do patients with a diagnosis of cancer receiving systemic anticancer therapy and using Resilience PRO have an improved quality of life? Researchers will compare patients using Resilience PRO plus care as usual to patients receiving care as usual only. Participants in the intervention arm will use Resilience PRO, a mobile phone application regularly asking participants about their symptoms. For clinically important symptoms, an alert is sent to the care team that can incorporate that information to timely adjust the care of the participants. Participants both in the control arm and in the intervention arm will further receive care as usual.

Participants needed: 1,458
Trial details
Phase: Phase 3Age: 18+Biological sex: AllType: InterventionalSponsor: ResilienceUpdated: Apr 3, 2026Locations: 36
Eligibility criteria

Age: Adults ≥ 18 years. [+5]

Age: Patients under 18 years of age. [+6]

Status: Not yet recruiting

Randomized Controlled Trial Comparing Remote Patient Monitoring vs Standard Care in IBD Patients Initiating or Changing Advanced Therapy

This clinical trial aims to evaluate whether GutyCare, a digital remote patient monitoring (RPM) solution, can enhance organizational outcomes while maintaining non-inferior clinical results in patients with inflammatory bowel disease (IBD) who are initiating or undergoing significant modifications in advanced therapy. The study compares standard care to an intervention involving the use of GutyCare, a mobile application that collects patient-reported outcomes related to symptoms. When clinically significant symptoms are identified, alerts are transmitted to the care team, facilitating timely and personalized therapeutic adjustments.

Participants needed: 116
Trial details
Phase: Phase 3Age: 18+Biological sex: AllType: InterventionalSponsor: ResilienceUpdated: Jun 29, 2025
Eligibility criteria

Diagnosed with Inflammatory bowel disease, either Crohn's disease or ulcerative... [+2]

Patients with altered intestinal continuity or function due to major abdominal s... [+3]