ClinicalTrials.gov
ClinicalTrials.gov Menu

Prevalence of Postpartum Depression in Hospital Jose E. Gonzalez

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.
ClinicalTrials.gov Identifier: NCT01658098
Recruitment Status : Unknown
Verified July 2012 by Dr Edgar Alejandro Tamez Cristerna, Hospital Universitario Dr. Jose E. Gonzalez.
Recruitment status was:  Not yet recruiting
First Posted : August 6, 2012
Last Update Posted : August 6, 2012
Sponsor:
Information provided by (Responsible Party):
Dr Edgar Alejandro Tamez Cristerna, Hospital Universitario Dr. Jose E. Gonzalez

Study Description
Go to 
Top of Page Study Description Study Design Groups and Cohorts Outcome Measures Eligibility Criteria Contacts and Locations More Information
Brief Summary:
This research will use the Edinburgh Scale Of Post partum depression to evaluate patients during their 4th to 6th after delivery, and the investigators will compare the results with those found in other countries with population with similar characteristics as ours

Condition or disease Intervention/treatment
Postpartum Depression Behavioral: edinburgh postpartum depression scale questionary

Study Design
Go to 
Top of Page Study Description Study Design Groups and Cohorts Outcome Measures Eligibility Criteria Contacts and Locations More Information

Study Type : Observational
Estimated Enrollment : 348 participants
Time Perspective: Prospective
Official Title: Prevalence of Postpartum Depression in the Jose E. Gonzalez Hospital, Using the Edinburgh Postpartum Depression Scale
Study Start Date : September 2012
Estimated Primary Completion Date : November 2012
Estimated Study Completion Date : February 2013

Resource links provided by the National Library of Medicine


Groups and Cohorts
Go to 
Top of Page Study Description Study Design Groups and Cohorts Outcome Measures Eligibility Criteria Contacts and Locations More Information

Group/Cohort Intervention/treatment
4-6 weeks after delivery
all patients on their 4th-6th weeks after delivery
 Behavioral: edinburgh postpartum depression scale questionary
the investigators will apply the qusetionary one time only in the period of time described previously


Outcome Measures
Go to 
Top of Page Study Description Study Design Groups and Cohorts Outcome Measures Eligibility Criteria Contacts and Locations More Information

Primary Outcome Measures :
  1. presence of postpartum depression [ Time Frame: 2 months ]

Secondary Outcome Measures :
  1. sociodemographic characteristics [ Time Frame: 2 months ]
    age

  2. sociodemographic characteristics [ Time Frame: 2 month ]
    level of education

  3. obstetrical background [ Time Frame: 2 month ]
    number of pregnancies

  4. medical background [ Time Frame: 2 month ]
    comorbid ities


Eligibility Criteria
Go to 
Top of Page Study Description Study Design Groups and Cohorts Outcome Measures Eligibility Criteria Contacts and Locations More Information

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:   Child, Adult, Older Adult
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population
348 patients on their 4th-6th week after delivery
Criteria

Inclusion Criteria:

  • patients on their 4th -6th week after delivery, who gave birth in our institution

Exclusion Criteria:

  • patients with previous diagnosis of psychiatric pathology
Contacts and Locations
Go to 
Top of Page Study Description Study Design Groups and Cohorts Outcome Measures Eligibility Criteria Contacts and Locations More Information

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01658098


Locations
Mexico
Hospital Universitario Dr Jose E. Gonzalez Not yet recruiting
Monterrey, Nuevo Leon, Mexico, 64460
Contact: Edgar Tamez, resident    01528183530442    julc316@hotmail.com   
Contact: sara Peña, resident    01528181231928    trysha_16@hotmail.com   
Sub-Investigator: Edgar Tamez, resident         
Sponsors and Collaborators
Hospital Universitario Dr. Jose E. Gonzalez
Investigators
Study Director: Emilio Treviño, specialist Consejo mexicano de ginecologia y obstetricia
More Information
Go to 
Top of Page Study Description Study Design Groups and Cohorts Outcome Measures Eligibility Criteria Contacts and Locations More Information

Publications:

Responsible Party: Dr Edgar Alejandro Tamez Cristerna, principal investigator, Hospital Universitario Dr. Jose E. Gonzalez
ClinicalTrials.gov Identifier: NCT01658098     History of Changes
Other Study ID Numbers: etamez
First Posted: August 6, 2012    Key Record Dates
Last Update Posted: August 6, 2012
Last Verified: July 2012

Keywords provided by Dr Edgar Alejandro Tamez Cristerna, Hospital Universitario Dr. Jose E. Gonzalez:
postpartum
depression
edinburgh postpartum depression scale
mexican population

Additional relevant MeSH terms:
Depression
Depressive Disorder
Depression, Postpartum
Behavioral Symptoms
 Mood Disorders
Mental Disorders
Puerperal Disorders
Pregnancy Complications