We are updating the design of this site. Learn more.
Show more
ClinicalTrials.gov
ClinicalTrials.gov Menu

Patient and Provider Outcomes of E-Learning Training in Collaborative Assessment and Management of Suicidality (CAMS)

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00905827
First Posted: May 21, 2009
Last Update Posted: April 24, 2015
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Collaborators:
Medical University of South Carolina
Washington Psychological Center
Information provided by (Responsible Party):
VA Office of Research and Development
Results First Submitted: December 29, 2014  
Study Type: Interventional
Study Design: Allocation: Randomized;   Intervention Model: Parallel Assignment;   Masking: Single (Outcomes Assessor);   Primary Purpose: Health Services Research
Condition: Suicide
Intervention: Behavioral: CAMS

  Participant Flow
  Hide Participant Flow

Recruitment Details
Key information relevant to the recruitment process for the overall study, such as dates of the recruitment period and locations
No text entered.

Pre-Assignment Details
Significant events and approaches for the overall study following participant enrollment, but prior to group assignment
No text entered.

Reporting Groups
  Description
Intervention 1: In-person CAMS Intervention: in-person CAMS training
Intervention 2: E-learning CAMS Intervention: e-learning CAMS training
Control Control: no training

Participant Flow:   Overall Study
    Intervention 1: In-person CAMS   Intervention 2: E-learning CAMS   Control
STARTED   70   69   73 
COMPLETED   70   69   73 
NOT COMPLETED   0   0   0 



  Baseline Characteristics
  Hide Baseline Characteristics

Population Description
Explanation of how the number of participants for analysis was determined. Includes whether analysis was per protocol, intention to treat, or another method. Also provides relevant details such as imputation technique, as appropriate.
comparison of three arms

Reporting Groups
  Description
Intervention 1: In-person CAMS Intervention: in-person CAMS training for providers
Intervention: E-training CAMS Intervention: e-training CAMS training for providers
Control Control: no training
Total Total of all reporting groups

Baseline Measures
   Intervention 1: In-person CAMS   Intervention: E-training CAMS   Control   Total 
Overall Participants Analyzed 
[Units: Participants]
 70   69   73   212 
Age, Customized 
[Units: Participants]
       
20-29 years   4   4   6   14 
30-39 years   22   22   23   67 
40-49 years   15   13   22   50 
50-59 years   19   22   18   59 
60-69 years   10   8   4   22 
Gender 
[Units: Participants]
       
Female   47   49   59   155 
Male   23   20   14   57 
Race/Ethnicity, Customized [1] 
[Units: Participants]
       
White   45   45   46   136 
African American   15   19   14   48 
Hispanic   0   2   1   3 
Other   6   1   4   11 
[1] Not all participants reported race, hence there may be differences in overall number
Profession 
[Units: Participants]
       
Psychiatrist   12   12   12   36 
Psychologist   16   13   18   47 
Midlevel Provider   42   44   43   129 


  Outcome Measures
  Show All Outcome Measures

1.  Primary:   Provider Self-efficacy and Beliefs About Suicidality   [ Time Frame: post-training ]

2.  Secondary:   Satisfaction With Training   [ Time Frame: post-training ]


  Serious Adverse Events


  Other Adverse Events


  Limitations and Caveats
  Hide Limitations and Caveats

Limitations of the study, such as early termination leading to small numbers of participants analyzed and technical problems with measurement leading to unreliable or uninterpretable data
Providers in this VISN may not be representative of providers in other VAMCs.


  More Information
  Hide More Information

Certain Agreements:  
All Principal Investigators ARE employed by the organization sponsoring the study.


Results Point of Contact:  
Name/Title: Kathryn Magruder
Organization: Department of Veteran Affairs
phone: 843-789-7280
e-mail: Kathryn.Magruder@va.gov


Publications of Results:

Responsible Party: VA Office of Research and Development
ClinicalTrials.gov Identifier: NCT00905827     History of Changes
Other Study ID Numbers: EDU 08-424
19016 ( Other Identifier: MUSC IRB )
First Submitted: May 19, 2009
First Posted: May 21, 2009
Results First Submitted: December 29, 2014
Results First Posted: January 9, 2015
Last Update Posted: April 24, 2015