NCT05053191

Brief Summary

The purpose of this study is to find out if a new training program for nurses called PACT (Partnership, Assessment, Care, and Transition) will be effective and relevant in helping nurses gain the skills needed to provide high-quality family-centered care. Family-centered care skills include engaging family caregivers as partners in patient care, and strengthening their capacity for caregiving by assessing family support needs and facilitating access to resources when needed. The study will also look at whether the quality of nurses' family-centered care skills is associated with improved outcomes for family caregivers. Both nurses and family caregivers will be enrolled in this study. Participants will be nurses/caregivers who care for advanced GI cancer patients admitted to Memorial Sloan Kettering.

Trial Health

75
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
84

participants targeted

Target at P50-P75 for not_applicable

Timeline
4mo left

Started Sep 2021

Longer than P75 for not_applicable

Geographic Reach
1 country

1 active site

Status
active not recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress94%
Sep 2021Sep 2026

Study Start

First participant enrolled

September 3, 2021

Completed
11 days until next milestone

First Submitted

Initial submission to the registry

September 14, 2021

Completed
8 days until next milestone

First Posted

Study publicly available on registry

September 22, 2021

Completed
5 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 3, 2026

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

September 3, 2026

Last Updated

September 19, 2025

Status Verified

September 1, 2025

Enrollment Period

5 years

First QC Date

September 14, 2021

Last Update Submit

September 18, 2025

Conditions

Keywords

Family CaregiverFamily Centered CareInpatient Oncology CareNursing Practices20-448Memorial Sloan Kettering Cancer Center

Outcome Measures

Primary Outcomes (1)

  • Frequency of nurses' use of family centered care practices

    Frequency of nurses' use of family centered care practices as observed during inpatient consultations with family caregivers

    30 days

Study Arms (1)

Nurses

EXPERIMENTAL

MSKCC day-shift nurses (Clinical Nurse I to IV) assigned to the GI inpatient unit (MH16) at the time of study, all of whom provide initial and ongoing assessment of patients' physical, psychosocial, cultural and informational needs

Behavioral: Partnership, Assessment, Care and Transition training intervention

Interventions

Partnership, Assessment, Care and Transition to psychosocial resources. Nurses who participate in PACT will receive 8 hours of training in a single, full-day workshop. We will train nurses in clusters of 10-12 nurses at one time, which will allow for cross-coverage with minimal disruption to workflow, and provide a more intimate, small-group learning environment.

Also known as: PACT
Nurses

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Nurses:
  • MSKCC day-shift nurses and/or night-shift nurses (Clinical Nurse I to IV) assigned to the GI inpatient unit (M16) at the time of study, all of whom provide initial and ongoing assessment of patients' physical, psychosocial, cultural and informational needs
  • Nurse is comfortable speaking and reading English as per self report
  • Family caregivers (FC) - Phase 1b:
  • Adult (≥18 yrs) family caregiver (family caregiver is defined here as any informal caregiver who is a relative, friend or legal representative) who self-identifies and/or is identified by the nursing staff as involved in the care of an MSK cancer patient who either:
  • is currently admitted to the M16 unity for at least 12 hours OR
  • has been discharged from the M16 unit within the last 2 weeks
  • English-speaking as per self-report
  • Only one FC per patient case will be invited to participate.
  • M16 Patients (chart review only):
  • Adult (≥18 yrs) cancer patient who is currently admitted in the M16 unit at Memorial Hospital for at least 12 hours o English speaking as per self-report

You may not qualify if:

  • Nurses:
  • Nurse plans to leave MSK or the GI unit within 3 months as per self-report
  • \[Phases 2-4\] Nurse refuses observation of consultations as per self-report
  • Family caregivers (FC) - Phase 1b:
  • FC's patient is deceased at time of consent

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Memorial Sloan Kettering Cancer Center

New York, New York, 10065, United States

Location

Related Links

MeSH Terms

Conditions

Gastrointestinal NeoplasmsGastrointestinal Diseases

Interventions

Restraint, Physical

Condition Hierarchy (Ancestors)

Digestive System NeoplasmsNeoplasms by SiteNeoplasmsDigestive System Diseases

Intervention Hierarchy (Ancestors)

Behavior ControlTherapeuticsImmobilizationInvestigative Techniques

Study Officials

  • Talia Zaider, PhD

    Memorial Sloan Kettering Cancer Center

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
OTHER
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

September 14, 2021

First Posted

September 22, 2021

Study Start

September 3, 2021

Primary Completion (Estimated)

September 3, 2026

Study Completion (Estimated)

September 3, 2026

Last Updated

September 19, 2025

Record last verified: 2025-09

Data Sharing

IPD Sharing
Will share

Memorial Sloan Kettering Cancer Center supports the international committee of medical journal editors (ICMJE) and the ethical obligation of responsible sharing of data from clinical trials. The protocol summary, a statistical summary, and informed consent form will be made available on clinicaltrials.gov when required as a condition of Federal awards, other agreements supporting the research and/or as otherwise required. Requests for deidentified individual participant data can be made beginning 12 months after publication and for up to 36 months post publication. Deidentified individual participant data reported in the manuscript will be shared under the terms of a Data Use Agreement and may only be used for approved proposals. Requests may be made to: crdatashare@mskcc.org.

Locations