Social Work Intervention Focused on Transitions (SWIFT)
Social Work Intervention Focused on Transitions Among At-Risk Older Adults
Study Overview
Status
Status
Conditions
Conditions
Intervention / Treatment
Intervention / Treatment
Study Type
Study Type
Enrollment (Actual)
Enrollment
Phase
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
California
-
Los Angeles, California, United States, 90089
- University of Southern California
-
Pasadena, California, United States, 91105
- Huntington Hospital
-
-
Participation Criteria
Eligibility Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
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
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Triple
Number of Arms
Arms and Interventions
Participant Group / ArmParticipant Group / Arm |
Intervention / TreatmentIntervention / 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
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
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
Sponsor
Sponsor
Collaborators
Collaborators
Study record dates
Study Major Dates
Study Start
Study Start
Primary Completion (Actual)
Primary Completion
Study Completion (Actual)
Study Completion
Study Registration Dates
First Submitted
First Submitted
First Submitted That Met QC Criteria
First Submitted That Met QC Criteria
First Posted (Estimated)
First Posted
Study Record Updates
Last Update Posted (Estimated)
Last Update Posted
Last Update Submitted That Met QC Criteria
Last Update Submitted That Met QC Criteria
Last Verified
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
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.
Clinical Trials on Depression
-
NCT07082998RecruitingDepression | Depression - Major Depressive Disorder | Depression Chronic | Depression in Adults | Depression Disorders | Depression Disorder
-
NCT05267340Active, not recruitingDepression Moderate | Depression Mild | Depression, Teen
-
NCT04211467WithdrawnDepression | Depression, Postpartum | Depression, Anxiety | Depression Moderate | Depression Severe | Clinical Depression | Depression in Remission | Depression, Endogenous | Depression Chronic
-
NCT07617467RecruitingAnxiety | Anxiety Depression | Depression Anxiety Disorder | Depression - Major Depressive Disorder
-
NCT06979544CompletedDepression, Postpartum | Postnatal Depression | Peripartum Depression | Depression, Post-Partum | Postpartum Depression (PPD) | Post-Natal Depression
-
NCT04504175CompletedTreatment Resistant Depression | Late Life Depression | Geriatric Depression | Refractory Depression | Therapy-Resistant Depression
-
NCT06374056Active, not recruitingDepression | Depression Moderate | Depression Severe | Depression Mild
-
NCT06809907RecruitingDepression | Depression Moderate | Depression Severe | Depression Mild
-
NCT07464886Recruiting
-
NCT07605975Completed
Clinical Trials on SWIFT home intervention
-
NCT07452523Active, not recruitingDisease Related Malnutrition
-
NCT05674747CompletedOnychomycosis of Toenail
-
NCT01705431Completed