Actively Recruiting

Age: 18Years +
All Genders
Healthy Volunteers
NCT06751641

Survey of Adult Participants Enrolled in Decentralized Clinical Trials

Led by Nantes University Hospital · Updated on 2025-01-16

200

Participants Needed

1

Research Sites

60 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Clinical trials (CTs) have become increasingly complex, requiring significant commitment from participants. Decentralized clinical trials (DCTs) offer an alternative by shifting some activities away from traditional sites to locations like the patient's home. This reduces the burden on participants, improves accessibility, and enhances recruitment and retention rates. DCTs leverage digital tools such as telemedicine, electronic consent, and wearable devices for data collection. These methods enable fewer site visits, lowering costs and integrating trials more seamlessly into participants' daily routines. This survey aims to assess the willingness of participants already enrolled in traditional CTs to engage in DCTs. Their prior experience with trial procedures allows them to provide valuable insights into the perceived benefits and feasibility of decentralized elements.

CONDITIONS

Official Title

Survey of Adult Participants Enrolled in Decentralized Clinical Trials

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults
  • Patients or healthy volunteers who can walk and are enrolled in an interventional clinical drug trial
  • Receiving trial treatments at the study site or at their home
Not Eligible

You will not qualify if you...

  • Individuals who have not agreed to participate in the survey
  • Individuals in clinical trials with procedures that cannot be done using decentralized methods

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

CHU Nantes

Nantes, France, 44000

Actively Recruiting

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Research Team

L

Laurent Flet, Pharm D

CONTACT

A

Alexandra Poinas

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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