- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02232126
Social Work Intervention Focused on Transitions (SWIFT)
November 8, 2023 updated by: Susan Enguidanos, University of Southern California
Social Work Intervention Focused on Transitions Among At-Risk Older Adults
In response to Program Announcement (PA)-09-164, "NIH Exploratory/Developmental Research Grant Program (R21) a randomized pilot study testing the efficacy of SWIFT: Social Work Intervention Focused on Transitions among at-risk older adults following hospital discharge to home.
This study is drawn from several observations.
First, transitions between care settings create elevated risk for poor outcomes and for readmission among older adults leaving the hospital for home largely due to fragmented care and poor communication.
Next, while few studies exist that test methods to improve transitions, those available are largely medically focused, using a nurse or advanced practice nurse in their approach.
Although evidence exists to support the effectiveness of these models, few have been replicated and none have been integrated into standard health care practice.
This may be attributed to several factors including the availability of the needed staff, the lack of existing structures to support these roles, and the costs of implementing these interventions.
Finally, a social work driven intervention may provide a replicable mechanism for bridging medical care, addressing psychosocial needs as well as medical needs, and improving linkages with community services while reducing care duplication.
This study aimed to test a structured social work transition intervention model to reduce rates of hospital readmission and medical service use while improving patient satisfaction with the care transition process.
A randomized pilot study was used to test a social work transitions model designed to improve care provided to frail older adults being discharged from the hospital to return to the community.
Eligible patients consenting to participate (n=181) were randomly assigned to either the social work transitions model intervention or usual care.
This project was conducted at Huntington Hospital, a 525-bed, nonprofit, community hospital located in Pasadena, California.
In an average year, Huntington Hospital has approximately 10,000 older adults discharged from their facility, 44% of who are 80 years old or older.
Those randomized to the intervention arm received up to six sessions from the social worker, at least one provided in the home.
The social work intervention was designed to overcome common problems following hospital discharge including medication review, discussion and planning around discharge instruction, assistance in scheduling follow up appointments, assessments of psychosocial and other support service needs and provision of linkages to address those needs.
Outcomes were measured three and six months following arrival at home, with an interim measure of satisfaction at 10 days following arrival at home, with measures including patient level of depression, pain, physical functioning, self-efficacy with disease management, and medical service use.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
181
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
California
-
Los Angeles, California, United States, 90089
- University of Southern California
-
Pasadena, California, United States, 91105
- Huntington Hospital
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
65 years and older (Older Adult)
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Age 65 or more
- English-speaking
- Community dwelling (own home, vs. assisted living facility/skilled care)
- Living within specified service net
- Cognitively intact (as measured by a score of 5 or more on the SPMSQ)
- Meeting at lease one or more of the following:
- Age 75 or more
- Taking 5 or more prescription medications
- Had at least one inpatient admission or emergency department visit in previous 6 months
Exclusion Criteria:
- Age 64 or younger
- Non-English speaking
- Diagnosed with end-stage renal disease
- Hospice recipient
- Diagnosis of Alzheimer's disease or severe dementia
- Residing in assisted living or skilled care facility
- Homeless
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Triple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Intervention
|
1 in-home assessment performed by study social worker, another in-home visit performed if needed.
Up to 4 telephone contacts performed by study social worker.
A maximum of 6 contacts
|
|
No Intervention: Usual Care
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
30-day Hospital Readmission
Time Frame: 30-days post hospitalization
|
The outcome measure is the number of readmissions experienced by participants in the Usual Care and Intervention groups within 30-days of their index discharge.
|
30-days post hospitalization
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
30-day Readmission Among Intervention Participants
Time Frame: 30-days
|
The outcome measure is the rate of 30-day readmissions among Intervention group participants that declined to receive the in-home social work intervention versus those Intervention group participants that received the in-home social work intervention.
|
30-days
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
February 1, 2011
Primary Completion (Actual)
October 1, 2013
Study Completion (Actual)
October 1, 2013
Study Registration Dates
First Submitted
August 25, 2014
First Submitted That Met QC Criteria
September 4, 2014
First Posted (Estimated)
September 5, 2014
Study Record Updates
Last Update Posted (Estimated)
November 9, 2023
Last Update Submitted That Met QC Criteria
November 8, 2023
Last Verified
November 1, 2023
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- UP-10-00372
- 5R21AG034557-02 (U.S. NIH Grant/Contract)
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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