Increasing Use of Mental Health Services (OpenDoor)
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|ClinicalTrials.gov Identifier: NCT00605358|
Recruitment Status : Completed
First Posted : January 31, 2008
Results First Posted : March 3, 2017
Last Update Posted : March 3, 2017
|Condition or disease||Intervention/treatment|
|Major Depression||Behavioral: Open Door intervention|
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||161 participants|
|Intervention Model:||Parallel Assignment|
|Primary Purpose:||Supportive Care|
|Official Title:||Increasing Use of Mental Health Services by Community Dwelling Adults With Depression|
|Study Start Date :||August 2007|
|Primary Completion Date :||January 2014|
|Study Completion Date :||January 2015|
Active Comparator: Open Door Intervention
Subjects who receive the Open Door Intervention will work with the study counselor to identify barriers to participation in mental health treatment, set goals, and problem-solve, in addition to receiving a referral.
Behavioral: Open Door intervention
Open Door intervention subjects will:
Other Name: West group
No Intervention: Services Referral
Subjects who do not receive the Open Door intervention will receive:
- The Primary Outcome is Engagement Defined as at Least One Visit With a Mental Health Provider Who Can Offer Treatment of Depression. [ Time Frame: 12 and 24 weeks ]
Engagement was defined as at least one visit with a mental health provider, due to the fact that in some treatment settings, the initial evaluation and the onset of treatment both took place in the first visit.
The primary outcome, engagement, was counted if the participant had engaged in mental health treatment by EITHER 12 weeks OR 24 weeks, based on research suggesting that older adults may take up to 6 months to follow through on a referral.
Therefore, while there is only a single primary outcome (engaged or not), it could be fulfilled at either of the two follow-up time points, at 12 or 24 weeks.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00605358
|United States, New York|
|Weill Cornell Medical College|
|White Plains, New York, United States, 10605|
|Principal Investigator:||Jo Anne Sirey, Ph.D.||Weill Medical College of Cornell University|