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

A Question Prompt Sheet for Depressive Outpatients

This study has been completed.
ClinicalTrials.gov Identifier:
First Posted: March 11, 2011
Last Update Posted: March 11, 2011
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.
Information provided by:
Technische Universität München
question prompt sheet for outpatients suffering from depression. effects on patient-doctor-communication during the consultation.

Condition Intervention
Depression Behavioral: question prompt sheet

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Health Services Research

Further study details as provided by Technische Universität München:

Estimated Enrollment: 100
Study Start Date: July 2010
Study Completion Date: March 2011
Primary Completion Date: March 2011 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: intervention
question prompt sheet
Behavioral: question prompt sheet
No Intervention: control
no question prompt sheet


Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.

Ages Eligible for Study:   18 Years to 65 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • 18-65 years
  • male and female patients
  • outpatients
  • informed consent

Exclusion Criteria:

  • poor German language skills
  Contacts and Locations
No Contacts or Locations Provided
  More Information

Responsible Party: PD Dr. Johannes Hamann
ClinicalTrials.gov Identifier: NCT01313013     History of Changes
Other Study ID Numbers: prompt1
First Submitted: March 9, 2011
First Posted: March 11, 2011
Last Update Posted: March 11, 2011
Last Verified: March 2011