NCT01334372

Brief Summary

This investigation is a feasibility study conducted in a VA outpatient treatment setting. The study is designed to test the feasibility of implementing a novel way of working with suicidal patients, the Collaborative Assessment and Management of Suicidality (CAMS). The primary purpose of the proposed project is to determine if it is possible to train clinicians working in the Mental Health Clinic at the Denver VA Medical Center (VAMC) to utilize this therapeutic framework. This project is extremely timely in relation to expectations of future increased clinical demands among potentially high-risk Operation Enduring Freedom/Operation Iraqi Freedom (OEF/OIF) veterans who may become suicidal in the years to come.

Trial Health

80
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
48

participants targeted

Target at P25-P50 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

February 1, 2007

Completed
2.8 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2009

Completed
1.4 years until next milestone

First Submitted

Initial submission to the registry

April 11, 2011

Completed
2 days until next milestone

First Posted

Study publicly available on registry

April 13, 2011

Completed
Last Updated

April 13, 2011

Status Verified

April 1, 2011

Enrollment Period

2.8 years

First QC Date

April 11, 2011

Last Update Submit

April 12, 2011

Conditions

Keywords

suicideveteransassessmentCAMS

Study Arms (2)

Treatment as Usual

NO INTERVENTION

Treatment as usual (TAU) outpatient care will consist of existing outpatient clinical practices utilized in the Mental Health Clinic.

CAMS

EXPERIMENTAL

First, as discussed above, suicidality is the focus of treatment rather than one of many symptoms being treated. Second is the emphasis on patient and therapist collaborating on treatment rather than the therapist dictating how therapy progresses. Beyond those two basic tenets, each therapist is free to utilize their current clinical skills to conduct psychotherapy.

Behavioral: CAMS

Interventions

CAMSBEHAVIORAL

First, as discussed above, suicidality is the focus of treatment rather than one of many symptoms being treated. Second is the emphasis on patient and therapist collaborating on treatment rather than the therapist dictating how therapy progresses. Beyond those two basic tenets, each therapist is free to utilize their current clinical skills to conduct psychotherapy.

CAMS

Eligibility Criteria

Age18 Years - 89 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Suicidality endorsed during the regular Mental Health intake interview or at the time of admission.
  • Over the age of 18 years.
  • New or returning patients to the VA MHC.
  • Living within the larger Denver metropolitan region during the duration of the treatment.
  • Willing to travel to the ECHCS Denver VAMC at times other than scheduled therapy appointments to complete follow-up assessment measures.

You may not qualify if:

  • Psychosis that would interfere with an individual's ability to provide informed consent.
  • Imminent suicidality with the need for immediate psychiatric hospitalization, as defined above in the Background section, at the time of MH intake.
  • Current involuntary status for psychiatric hospitalization.
  • Inability to adequately respond to questions regarding the informed consent procedure. See Special Consent Issues section below.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Visn 19 Mirecc

Denver, Colorado, 80220, United States

Location

MeSH Terms

Conditions

Suicidal IdeationSuicide

Condition Hierarchy (Ancestors)

Self-Injurious BehaviorBehavioral SymptomsBehavior

Study Officials

  • Lisa A Brenner, PhD

    VISN 19 MIRECC

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Sponsor Type
FED

Study Record Dates

First Submitted

April 11, 2011

First Posted

April 13, 2011

Study Start

February 1, 2007

Primary Completion

December 1, 2009

Last Updated

April 13, 2011

Record last verified: 2011-04

Locations