Status:
COMPLETED
Integrated Intervention for Caregivers--Pilot RCT
Lead Sponsor:
Wake Forest University Health Sciences
Collaborating Sponsors:
Duke University
University of Rochester
Conditions:
Distress; Maternal
Self Efficacy
Eligibility:
All Genders
13+ years
Phase:
NA
Brief Summary
Adolescents who have been hospitalized for suicidal behavior are at risk for engaging in additional suicidal behavior. After hospitalization, parents or guardians are typically asked to be responsible...
Detailed Description
Adolescents who have been hospitalized for suicidal behavior are at high risk for engaging in additional suicidal behavior. Following hospitalization, parents or guardians are typically tasked with he...
Eligibility Criteria
Inclusion
- Biological, adoptive, or step- parent (step-parent defined as by marriage or live-in partner of at least 5 years) of an adolescent. If an adolescent has more than one parent, investigators will ask parents to designate the primary contact or participant for this study (only one parent for an adolescent may participate).
- The adolescent is 13-19 years of age
- The adolescent was psychiatrically hospitalized due to any range of suicidal behaviors (i.e., suicide attempt, interrupted suicide attempt, aborted suicide attempt) in the last two weeks
- The parent lives with the adolescent
- The parent has a cell phone and is capable of texting (i.e., has knowledge of how to text and has a data plan that allows for texting)
Exclusion
- Parents whose primary language is not English and are unable to read or speak English, as all materials will be initially developed in English only
- Parents who have a reported intellectual disability (per inpatient staff)
- Parents whose adolescent is not discharged directly home (e.g., adolescent is sent to a group home, residential treatment facility, or home of a relative following hospitalization)
- Adolescents who have an intellectual disability (per inpatient staff or as reflected by current school placement) or have active psychosis, as the needs of both parent and youth may be different than those without an intellectual disability or active psychosis and are not specifically addressed in the proposed developing intervention
Key Trial Info
Start Date :
May 4 2021
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
December 14 2022
Estimated Enrollment :
90 Patients enrolled
Trial Details
Trial ID
NCT03487627
Start Date
May 4 2021
End Date
December 14 2022
Last Update
December 30 2022
Active Locations (1)
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1
Wake Forest Health Sciences
Winston-Salem, North Carolina, United States, 27157