NCT02354482

Brief Summary

Funded by the Patient Centered Outcome Research Institute (PCORI), nationally recognized leaders in health care and research methods are partnering with patients and caregivers to evaluate the effectiveness of current efforts at improving care transitions and develop recommendations on best practices for patient-centered care transitions and guidance for spreading them across the U.S.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
7,939

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Mar 2015

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
completed

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

First Submitted

Initial submission to the registry

January 29, 2015

Completed
5 days until next milestone

First Posted

Study publicly available on registry

February 3, 2015

Completed
26 days until next milestone

Study Start

First participant enrolled

March 1, 2015

Completed
4.2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 30, 2019

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

June 30, 2019

Completed
5 months until next milestone

Results Posted

Study results publicly available

November 26, 2019

Completed
Last Updated

November 26, 2019

Status Verified

November 1, 2019

Enrollment Period

4.2 years

First QC Date

January 29, 2015

Results QC Date

October 1, 2019

Last Update Submit

November 4, 2019

Conditions

Outcome Measures

Primary Outcomes (2)

  • Hospital Readmission

    Readmission to the hospital within 30 days of discharge.

    30 days post hospital discharge

  • Emergency Department (ED) Visit

    Visit to the ED within 30 days of hospital discharge.

    30 days post hospital discharge

Study Arms (1)

Diverse, high-risk patient populations

Behavioral: Patient Communication and Care ManagementBehavioral: Home-Based Trust, Plain Language, and CoordinationBehavioral: Hospital-Based Trust, Plain Language, and CoordinationBehavioral: Patient/Caregiver Assessment and Provider Information ExchangeBehavioral: Assessment and Teach BackOther: Standard of Care (Reference)

Interventions

Received the following Transitional Care strategies: 1. Helpful Health Care Contact OR Symptom Management 2. Post-discharge Care Consultation 3. Patient Goal/Preference Assessment 4. Plain Language Communication in Hospital 5. Plain Language Communication at Home 6. Transition Summary for Patients and Family Caregivers

Diverse, high-risk patient populations

Received the following Transitional Care Strategies: 1. Transition Team 2. Home visits 3. Plain Language Communication at Home 4. Promote Trust at Home 5. Referral to Community Services 6. Follow-up Appointment

Diverse, high-risk patient populations

Received the following Transitional Care Strategies: 1. Post-discharge care consultation 2. Identify High-Risk Patients and Intervene 3. Medication Reconciliation 4. Plain Language Communication in Hospital 5. Promote Trust in the Hospital 6. Transition Summary for Patients and Family Caregivers

Diverse, high-risk patient populations

Received the following Transitional Care Strategies: 1. Patient Goal/Preference Assessment 2. Identify High-Risk Patients and Intervene 3. Timely Exchange of Critical Patient Information among Providers 4. Patient/Family Caregiver Transitional Care Needs Assessment

Diverse, high-risk patient populations

Received the following Transitional Care Strategies: 1. Post-discharge care consultation 2. Language Assessment 3. Teach Back for Information and Skills

Diverse, high-risk patient populations

No specific Transitional Care Strategy

Diverse, high-risk patient populations

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

Project ACHIEVE will focus on Medicare fee-for-services beneficiaries and study diverse high risk patient populations, including those with: 1) multiple chronic conditions; 2) mental health issues; 3) rural area domicile; 4) limited English proficiency or low health literacy; 5) low socioeconomic status; 6) Medicare and Medicaid dual eligible; 7) disabled and younger than 65.

You may qualify if:

  • diverse high risk patient populations, including those with:
  • multiple chronic conditions
  • mental health issues
  • rural area domicile
  • limited English proficiency or low health literacy
  • low socioeconomic status
  • Medicare and Medicaid dual eligible
  • disabled and younger than 65.

You may not qualify if:

  • children
  • non-Medicare patients
  • Under police custody
  • Under suicide watch
  • In-hospital death
  • Transferred (not discharged) to another acute care hospital
  • Discharged against medical advice
  • Admission for primary diagnosis of psychiatric conditions
  • Admission for rehabilitation
  • Admission for medical treatment of cancer

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

UK Healthcare

Lexington, Kentucky, 40536, United States

Location

Related Publications (1)

  • Li J, Brock J, Jack B, Mittman B, Naylor M, Sorra J, Mays G, Williams MV; Project ACHIEVE Team. Project ACHIEVE - using implementation research to guide the evaluation of transitional care effectiveness. BMC Health Serv Res. 2016 Feb 19;16:70. doi: 10.1186/s12913-016-1312-y.

MeSH Terms

Interventions

Restraint, PhysicalStandard of Care

Intervention Hierarchy (Ancestors)

Behavior ControlTherapeuticsImmobilizationInvestigative TechniquesQuality Indicators, Health CareQuality of Health CareHealth Services AdministrationHealth Care Quality, Access, and Evaluation

Results Point of Contact

Title
Jessica Clouser
Organization
University of Kentucky

Study Officials

  • Mark V Williams, MD

    University of Kentucky

    PRINCIPAL INVESTIGATOR

Publication Agreements

PI is Sponsor Employee
Yes

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

January 29, 2015

First Posted

February 3, 2015

Study Start

March 1, 2015

Primary Completion

April 30, 2019

Study Completion

June 30, 2019

Last Updated

November 26, 2019

Results First Posted

November 26, 2019

Record last verified: 2019-11

Data Sharing

IPD Sharing
Will not share

Locations