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Using Caring Contacts to Reduce Psychiatric Morbidity Following Hospitalization During the COVID-19 Pandemic

S

Sunnybrook Health Sciences Centre

Status

Completed

Conditions

Psychiatric Hospitalization

Treatments

Other: Caring Contacts

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

Subjects will be recently discharged patients from Sunnybrook Inpatient Psychiatry Unit. Subjects will be randomized in a 1:1 ratio to either the Caring Contact intervention or usual care. 75 subjects will be enrolled in each arm. In additional to usual discharge-related care, subjects in the caring contact group will receive brief emails that convey a message of hope and provide resources. These emails will be sent on days 4, 21, and 56 post-discharge. The specific content of these emails will be pre-determined varying slightly by time point. In contrast, the control group will only receive usual discharge-related care, including discharge planning and also a sheet of resources normally provided to patients. A widely used and validated measure will be employed to assess depression and anxiety symptoms. The 25-item self-report Hopkins Symptom Checklist will be emailed to all subjects at baseline, day 4, 21, and 56 post-discharge, along with the Caring Contact communication. It is hypothesized that there will be a significantly greater reduction in mental health symptoms among patients receiving Caring Contacts compared to those who receive usual care.

Enrollment

102 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Provision of written informed consent
  • Inpatient status in Sunnybrook Inpatient Psychiatry Unit at time of recruitment
  • Have an email or mailing address
  • Ability to read and understand English
  • The ability to understand and comply with the requirements of the study and capable of providing informed consent

Exclusion criteria

  • A primary Major Neurocognitive Disorder diagnosis

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

102 participants in 2 patient groups

Caring Contacts Group
Experimental group
Treatment:
Other: Caring Contacts
Standard Treatment Group
No Intervention group

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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