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A Trial of effectIveness of a Smart Sensor for Continence Care: the ARCTICC Study

NCT02511314 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 89

Last updated 2021-01-25

No results posted yet for this study

Summary

The purpose of this study is to compare the use of an electronic incontinence identification system with nursing home support (Tena Identifi) versus usual care on the quality, resource use and outcomes of continence care for older residents of nursing care homes.

Conditions

Interventions

DEVICE

TENA Identifi

TENA Identifi

Sponsors & Collaborators

  • SCA Hygiene Products, AB

    collaborator UNKNOWN

  • University of Alberta

    lead OTHER

Principal Investigators

  • Adrian S Wagg, MD · University of Alberta

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-01-02
Primary Completion
2019-10-30
Completion
2020-03-30

Countries

  • Canada

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02511314 on ClinicalTrials.gov