Community Academic Profiles

Craig S. Rosen

Telephone Care for Veterans With PTSD

Contact Information

Central Contact:

Craig Rosen (650) 493-5000 22812
VA Palo Alto Health Care System 3801 Miranda Avenue Palo Alto, CA 94304

Primary Contact:

Craig Rosen (650) 493-5000 22812
To view all clinical trials at Stanford, please see the Clinical Trials Directory.

Brief

Ths is a study of telephone support for veterans who are discharging from residential PTSD treatment. We hope to learn whether providing additional case management by telephone helps veterans during their transition from residential treatment to outpatient care.

Recruiting Status:

Recruiting

Stanford Recruiting Status:

Intervention(s):

  • Behavior: Telephone case monitoring

Phase:

N/A

Eligibility

Ages Eligible for Study:

18 years to Any Age

Genders Eligible for Study:

Male and Female

Health of Volunteers:

People with the conditions listed in this trial can participate as controls.

Key Inclusion Criteria:

VA patients with a PTSD diagnosis entering PTSD residential treatment with an intended length of stay of 15 days or longer (patients in brief evaluation or acute stabilization tracks will not be included, as their discharge plan may include readmission to residential treatment within a few months).

Key Exclusion Criteria:

a) Patients discharging from residential treatment within four days of admission(insufficient time to consent and assess them); b) Active Duty military personnel; c) Patients transferred from residential care to an inpatient medical unit due to emergent medical problems; d) patients with traumatic brain injury or other organic impairment that compromises capacity to consent

Additional Study Details

Official Title:

Telephone Case Monitoring for Veterans With PTSD

Anticipated start date:

4/1/2006

Lead Sponsor:

Department of Veterans Affairs

Investigator(s):

Study Type:

Interventional

Purpose:

Treatment

Allocation:

Randomized

Masking:

Single Blind

Control:

none

Assignment:

Single Group

Endpoints:

Efficacy

Primary Outcomes:

  • a) violence, substance use, PTSD symptoms; b) time to rehospitalization; c) costs

Secondary Outcomes:

  • d) depressive symptoms, subjective quality of life

Total Number to be Enrolled:

1200

Total Number to be Enrolled at Stanford:

0

More Information

Trial Unique Id: SU-07232007-529

Locations & Contacts

Stanford Locations & Contacts:

Central Contact for This Study:

Craig Rosen (650) 493-5000 22812
VA Palo Alto Health Care System 3801 Miranda Avenue Palo Alto, CA 94304

Primary Contact:

Craig Rosen (650) 493-5000 22812

Non-Stanford Locations:

This study is being conducted at multiple locations, including non-Stanford locations.

This listing was last updated:

1/16/2009

PLEASE NOTE:

Study Coordinators and Research Nurses cannot give medical advice over the phone. Telephone numbers are provided for obtaining additional information on specific clinical research trials only. If you have specific questions which require clinical expertise, please call your primary care physician. If you do not have a primary care physician please feel free to call the SHC Physician Referral Service at (800) 756-9000 or send an email.

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