NCT03879291

Terminated

Assessment of Utility of accelerateIQ in the Care of Patient...

Karen Larimer Source

Karen Larimer

ClinicalTrials.gov

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Other study identifiers

Sponsor study identifier

CTP-010

Study Type

observational

Actual enrollment (reported)

5

Locations

1 country

Sites

1

Timeline

Study Start

January 9, 2019

Actual (reported)

Primary Completion

December 30, 2019

Actual (reported)

Study Completion

December 30, 2019

Actual (reported)

Brief Summary

The proposed study seeks to assess the performance of continuous biosensor data and machine learning analytics in assessment of health patient status in a pulmonary rehabilitation program. It is hypothesized that using continuous physiologic biosensor data and machine learning analytics to detect changes in physiology may play a role in managing patients in the pulmonary rehabilitation setting.

Registry Overview

Registry-reported information. Elapsed time and enrollment totals alone do not measure study progress or recruitment pace.

Recruitment status: terminated
Actual enrollment (reported): 5 participants
Study completion date: December 30, 2019
Actual (reported)
Listed locations: 1 countries · 1 sites

Trial Relationships

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Some registry-reported names shown below are not yet linked in this graph.

Study Timeline

Dates and qualifiers reported by the registry. Estimated dates do not confirm that a milestone has occurred.

Study Start
January 9, 2019
Actual (reported)
First Submitted
March 14, 2019
Actual (reported)
First Posted
March 18, 2019
Actual (reported)
Primary Completion
December 30, 2019
Actual (reported)
Study Completion
December 30, 2019
Actual (reported)

Last Updated: March 16, 2020
Status Verified: March 2020
Last Update Submitted: March 12, 2020

Conditions

COPD Pulmonary Rehabilitation

Outcome Measures

Primary Outcomes (1)

Clinical Utility
Correlation of reported health events with the multivariate change index
90 days

Interventions

pinpointIQOther

The study will utilize physIQ's multivariate analytical methods that detect vital sign relationship changes compared to a patient's individual baseline. Changes in vital signs relationships may be indicative of current or future important clinical events. These changes are indicated through the Multivariate Change Index (MCI), which is a scalar index between 0 and 1, where values close to 0 indicate no significant change from baseline and values close to 1 indicated greater changes from baseline

Registry-reported names are shown in full. Names without a link have not yet been matched to a Syfrah profile.

Eligibility Criteria

Age40 Years+

Sexall

Age GroupsAdult (18-64), Older Adult (65+)

Sampling MethodNon-Probability Sample

Study Population

The study population will be patients diagnosed with COPD participating in a pulmonary rehabilitation program.

You may qualify if:

Male or female, at least 40 years of age;

Sponsors & Collaborators

Sunovian
Type not reportedcollaborator
Karen Larimer
Industrylead

Study Sites (1)

NorthShore University Health System

Evanston, Illinois, 60201, United States

MeSH Terms

Conditions

Pulmonary Disease, Chronic Obstructive

Condition Hierarchy (Ancestors)

Lung Diseases, ObstructiveLung DiseasesRespiratory Tract DiseasesChronic DiseaseDisease AttributesPathologic ProcessesPathological Conditions, Signs and Symptoms

Enrollment

5 participants (actual enrollment reported by the registry).

Study Design

Study Type: observational
Observational Model: COHORT
Time Perspective: PROSPECTIVE
Sponsor Type: INDUSTRY
Responsible Party: SPONSOR INVESTIGATOR
PI Title: Director of Clinical Development

Study Record Dates

First Submitted

March 14, 2019

First Posted

March 18, 2019

Study Start

January 9, 2019

Actual (reported)

NCT07747571

Factors Associated With Acceptance of Home-Based Pulmonary Telerehabilitation in COPD

Not Yet Recruiting

NCT04004689

6-minute Stepper Test and Pulmonary Rehabilitation in Patients With Severe to Very Severe Chronicle Obstructive Pulmonary Disease

Unknown

NCT03295474

Telemonitoring in Pulmonary Rehabilitation: Feasibility and Acceptability of a Remote Pulse Oxymetry System.

Completed

NCT03489642

Innovative Pulmonary Rehabilitation Telehealth Program for Improving COPD Patient Outcomes

Not ApplicableCompleted

NCT03801330

Inspiration Point-A Digital Pulmonary Rehabilitation Tool Management Interventions

Not ApplicableCompleted

NCT02999685

Home-based Health Management of Chronic Obstructive Lung Disease (COPD) Patients

Not ApplicableCompleted

Diagnosis of Chronic Obstructive Pulmonary Disease (COPD);

Enrolled in the study site's 12-week pulmonary rehabilitation program;

Capable of completing a 6-minute walk test;

Willing and able to comply with scheduled protocol procedures and follow up;

Signed and dated informed consent and HIPAA materials indicating that the patient has agreed to participate in this study and has been informed of all pertinent aspects of the trial.

You may not qualify if:

Patient has cognitive or physical limitations that, in the opinion of the investigator, limit the patient's ability to utilize the System as instructed;
Patient is actively enrolled in another clinical investigation that, in the opinion of the investigator, interferes with or compromises either that patient's ability to participation in this study or the ability for the study to generate results;
Patients who have implanted defibrillators or pacemakers;
Patient is allergic to hydrocolloid adhesive;
Patient does not speak English.

Contact the study team to confirm eligibility.

Primary Completion

December 30, 2019

Actual (reported)

Study Completion

December 30, 2019

Actual (reported)

Last Updated

March 16, 2020

Record last verified: 2020-03

Data Sharing

IPD Sharing: Will not share

Source record

Download the complete ClinicalTrials.gov record imported by Syfrah, including fields not shown in this page. The registry may contain a newer revision.

Source: ClinicalTrials.gov.

JSON downloads include source attribution and retrieval details alongside the unchanged original record or the separately normalized values.

Registry identifier: NCT03879291
Data provider: ClinicalTrials.gov
Source updated: 2020-03-16
Normalization version: ctgov-legacy-1

Open registry record

Source retrieved: 2026-10-25 22:21:50 UTC

Locations

US(1)

Study Stopped

Assessment of Utility of accelerateIQ in the Care of Patients Participating in a Pulmonary Rehabilitation Program

Brief Summary

Registry Overview

Trial Relationships

Study Timeline

Study Start

First Submitted

First Posted

Primary Completion

Study Completion

Conditions

Outcome Measures

Primary Outcomes (1)

Interventions

Eligibility Criteria

You may qualify if:

Sponsors & Collaborators

Study Sites (1)

MeSH Terms

Conditions

Condition Hierarchy (Ancestors)

Enrollment

Study Design

Study Record Dates

You may not qualify if:

Data Sharing

Source record

Locations

Brief Summary

Registry Overview

Trial Relationships

Related Scientific Literature

Study Timeline

Study Start

First Submitted

First Posted

Primary Completion

Study Completion

Conditions

Outcome Measures

Primary Outcomes (1)

Interventions

Eligibility Criteria

You may qualify if:

Sponsors & Collaborators

Study Sites (1)

MeSH Terms

Conditions

Condition Hierarchy (Ancestors)

Enrollment

Study Design

Study Record Dates

You may not qualify if:

Data Sharing

Source record

Locations