Skip to main content
Clinical Trials/NCT01581983
NCT01581983
Completed
Phase 1

Mindfulness Meditation Format Pilot Study

Oregon Health and Science University1 site in 1 country8 target enrollmentApril 2012

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Posttraumatic Stress Disorder
Sponsor
Oregon Health and Science University
Enrollment
8
Locations
1
Primary Endpoint
Beck Depression Inventory
Status
Completed
Last Updated
10 years ago

Overview

Brief Summary

The purpose of this study is to assess feasibility of an internet and individual format of mindfulness meditation in people with posttraumatic stress disorder (PTSD) and depression symptoms

Detailed Description

Internet and individual formats of mindfulness meditation have not been previously evaluated. In order establish feasibility of such formats a pilot study is need. The current study will randomize up to 20 people with PTSD and depression symptoms and evaluate changes in PTSD and depression symptoms from before to after the internet and individual mindfulness meditation interventions.

Registry
clinicaltrials.gov
Start Date
April 2012
End Date
June 2015
Last Updated
10 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Helane Wahbeh

Assistant Professor

Oregon Health and Science University

Eligibility Criteria

Inclusion Criteria

  • Good general health
  • Age 25-65
  • Access to internet
  • PTSD symptoms (score \>14 on PTSD screen)
  • Depression symptoms (endorsement of one question on depression screen)
  • Stable on medications six weeks prior to the study
  • Willing to be stable on medications during study

Exclusion Criteria

  • Significant potentially life-limiting acute medical illness
  • Risk for suicide
  • \>2 drinks/day of alcohol and street drug use besides marijuana
  • Current daily meditation practice

Outcomes

Primary Outcomes

Beck Depression Inventory

Time Frame: Change from Baseline to Week 7

The Beck Depression Inventory will be administered immediately before their first intervention session and within one week of their last intervention session. The primary outcome is the change in score on this instrument from baseline to week 7.

Posttraumatic Stress Disorder Checklist

Time Frame: Change from baseline to week 7.

The Posttraumatic Stress Disorder Checklist will be administered immediately before their first intervention session and within one week of their last intervention session. The primary outcome is the change in score on this instrument from baseline to week 7.

Study Sites (1)

Loading locations...

Similar Trials