Depression Clinical Trial
Official title:
Care Transitions for Medically Ill Patients With Depression
Verified date | July 2019 |
Source | Cedars-Sinai Medical Center |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Aim 1: To collect data on a Depression Care Transition (DCT) program's association with
self-care behaviors as measured by medication adherence and clinic visit attendance, after
discharge. Hypothesis 1: Compared with usual care, patients who receive the DCT intervention
will have significantly greater medication adherence and clinic visit attendance, at 30, 90,
and 365 days after discharge.
Aim 2: To collect data on DCT's association with clinical/health outcomes as measured by
depression severity, functional status, and overall physical and mental health, after
discharge. Hypothesis 2: Compared with usual care, patients who receive the DCT intervention
will have significantly larger improvements in depression severity, functional status, and
overall physical & mental health at 30, 90, and 365 days after discharge.
Aim 3: To collect data on DCT's association with utilization outcomes as measured by
readmissions, length of subsequent hospital stays, and cost of care, after discharge.
Hypothesis 3: Compared with usual care, patients who receive the DCT intervention will have
significantly lower hospital readmissions, shortened length of subsequent hospital stays and
lower cost of care, at 30, 90, and 365 days of discharge.
Leading the research team are a psychiatrist (Dr. IsHak - PI) and a hospitalist (Dr. Nuckols
- Co-I) with an advanced and well-established track record of health services
research/scholarship in the fields of depression, outcome measurement, and economic
implications of improving the quality and safety of health care.
Status | Withdrawn |
Enrollment | 0 |
Est. completion date | December 31, 2021 |
Est. primary completion date | December 31, 2019 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Participants older than the age of 18, admitted to Cedars-Sinai Medical Center, English speaking, and answers "yes" to either question on the PHQ-2 instrument. Exclusion Criteria: - Participants under the age of 18, non-English speaking, and does not answer "yes" to either question on the PHQ-2 instrument. |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Cedars-Sinai Medical Center |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Transitional Care | Patients in the DCT intervention will have a Transitional Care Social Worker (TCSW) who will maintain daily phone contact, home visits, and will attend with the patient medical and psychiatric appointments for an average of three months following discharge. Patients in the usual care group will proceed as usual (scheduled follow-up visits). These subjects will also be asked to complete questionnaires relating to quality of life and physical and mental health status. | 365 days | |
Secondary | Depression Surveys | All patients who are admitted to CSMC are screened for depression using the PHQ instrument (Kroenke, Spitzer, & Williams, 2001). Patients are asked two questions about frequent occurrence of cardinal depressive symptoms - sadness and anhedonia - and provide yes/no answers to the intake nurse (PHQ-2). If patients answer, "yes" to either question, they are administered the complete PHQ-9 instrument. Per the CSMC depression screening protocol, if patients score >12 on the PHQ-9, a social worker evaluation, and notification of the admitting physician and psychiatry, will take place. The subjects will be identified through the psychiatrist who will discuss the risks and benefits of study participation, and assess the patient's interest in the study. | 365 days |
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