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Recruiting Not applicable Interventional

Pip Care to Improve Surgical Patient Outcomes

ClinicalTrials.gov ID: NCT06661291

Public ClinicalTrials.gov record NCT06661291. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 6, 2026, 6:49 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Utilization of Digital Health Platform Plus Live Coaching Improves Surgical Patients Outcomes - Phase II

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Pip Care is developing a personalized, interactive surgical journey platform with a live health coach that works directly with health systems to optimize the perioperative care process. Our Health Insurance Portability and Accountability Act (HIPAA)-compliant platform, Pip, can be integrated into any electronic medical record (EMR), thus alleviating the administrative burden by making operational workflows more efficient. The PIP empowers patients and their families to be more involved in their care by breaking down a patient's healthcare plan into definable, easy-to-understand, and easy-to-complete tasks. Additionally, a health coach completes a health intake to create a personalized perioperative care plan, meets regularly with the patient to encourage goal accomplishment, and facilitates care coordination. This project has 2 phases; Phase I is to assess usability of the Pip Care platform in surgical patients, Phase II is a RCT (Randomized Controlled Trial) to assess surgical clinical outcomes while using Pip compared to standard of care.

Study identification

NCT ID
NCT06661291
Recruitment status
Recruiting
Study type
Interventional
Phase
Not applicable
Lead sponsor
University of Pittsburgh
Other
Enrollment
1,300 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Oct 12, 2025
Primary completion
Aug 31, 2028
Completion
Aug 31, 2028
Last update posted
Oct 27, 2025

2025 – 2028

United States locations

U.S. sites
8
U.S. states
1
U.S. cities
2
Facility City State ZIP Site status
UPMC Jameson Hospital New Castle Pennsylvania 16105 Recruiting
UPMC East Hospital Pittsburgh Pennsylvania 15146 Recruiting
UPMC Horizon Pittsburgh Pennsylvania 15213 Recruiting
UPMC Magee Womens Hospital Pittsburgh Pennsylvania 15213 Recruiting
UPMC Presbyterian Hospital Pittsburgh Pennsylvania 15213 Recruiting
UPMC St. Margaret Pittsburgh Pennsylvania 15213 Recruiting
UPMC Shadyside Hospital Pittsburgh Pennsylvania 15232 Recruiting
UPMC Passavant Hospital Pittsburgh Pennsylvania 15237 Recruiting

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06661291, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Oct 27, 2025 · Synced Sep 6, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT06661291 live on ClinicalTrials.gov.

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