Patient acceptability and technical robustness of the Elucid Pill Connect system for use in clinical trials

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON19951

Enrollment

Registered

2019-06-27

Start date

2019-06-28

Completion date

Unknown

Last updated

2024-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Provision of the Elucid Pill Connect System

Eligibility

Inclusion criteria

Inclusion criteria: (1) age >18 years, (2) own an Android or Iphone phone with the required OS versions, (3) are able to operate the mobile phone themselves and (4) provide informed consent.

Exclusion criteria

Exclusion criteria: None

Design outcomes

Primary

Measure	Time frame
Percentage of pills dispensed according to intended dosing schedule	—

Secondary

Measure	Time frame
User acceptance (measured with the System Usability Scale and a self-designed questionnaire), investigator acceptance, technical validation (correct logging of dispense data, timing, battery life, sending of reminders, locking and temperature) and comparison with self-reported adherence according to the MARS questionnaire	—

Contacts

Public ContactJob F.M. van Boven

University Medical Center Groningen

j.f.m.van.boven@umcg.nl+31503617893

Outcome results