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| Name | Class |
|---|---|
| Centers for Disease Control and Prevention | FED |
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Specific aim #1: To assess the study team's ability to recruit subjects in this cohort and to successfully complete follow-up assessments by phone or mail.
Hypothesis: Over 50% of eligible subjects will enroll in the observational study, and 70% of follow-up assessments will be successfully completed.
Specific aim #2: To determine the natural history of hopelessness, ongoing suicidal thoughts, and optimism in subjects at 2, 4 and 8 weeks after discharge.
Hypothesis: Subjects will continue to have moderate levels of hopelessness, suicidal thoughts, and optimism at follow-up assessments.
Contact information. On the day of enrollment, contact information (address, phone number) will be obtained from the subject. Subjects will also be asked to provide the contact information for a family member or friend who the study team may contact in case of emergency or if unable to get in touch with subject at follow up. Subjects unable to provide contact information for at least one family member will not be enrolled.
Baseline evaluation.
On the date of enrollment, study staff will obtain two types of information:
Baseline clinical characteristics. Study staff will obtain specific clinical variables from the patient to gather information about variables that could impact levels of hopelessness/optimism after discharge. These variables include: age, gender, # of prior admissions [zero, 1-5, more than 5], presence of substance use disorder (assessed via inpatient chart review), admission for suicide attempt or suicidal ideation only, and involvement in exercises that can increase feelings of well-being like gratitude, forgiveness, using one's personal strengths, and acts of kindness.
Baseline outcome measures: Study staff will also administer six instruments:
This evaluation should take approximately 20-30 minutes.
Follow-up assessments.
Follow-up assessments will occur by phone or mail at 2 weeks, 4 weeks and 8 weeks. Similar to initial assessments, the follow-up assessments will have two components:
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Suicidal ideation/behavior |
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| Measure | Description | Time Frame |
|---|---|---|
| Ability to recruit and retain subjects in this cohort | Number of subjects who enroll in the study, and number of subjects who complete phone or written follow-ups at each time point. | 2 years |
| Measure | Description | Time Frame |
|---|---|---|
| Change in the natural history of hopelessness, suicidal thoughts, and optimism | Changes in scores between baseline and 2/4/8 weeks after discharge. Rates of readmission to hospital, suicidal thoughts, and non-suicidal self-harming behaviors | 2, 4, and 8 weeks |
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Inclusion criteria:
Exclusion criteria:
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Patients admitted to the Inpatient Psychiatric Unit at Massachusetts General Hospital
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| Name | Affiliation | Role |
|---|---|---|
| Jeff C Huffman, MD | Massachusetts General Hospital | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Massachusetts General Hospital | Boston | Massachusetts | 02114 | United States |
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| ID | Term |
|---|---|
| D013406 | Suicide, Attempted |
| D059020 | Suicidal Ideation |
| D013405 | Suicide |
| ID | Term |
|---|---|
| D016728 | Self-Injurious Behavior |
| D001526 | Behavioral Symptoms |
| D001519 | Behavior |
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