Status:

COMPLETED

Effect of Exercise and Wellness Interventions on Preventing Postpartum Depression

Lead Sponsor:

University of Minnesota

Collaborating Sponsors:

National Institute of Mental Health (NIMH)

Conditions:

Postpartum Depression

Eligibility:

FEMALE

21-45 years

Phase:

NA

Brief Summary

The purpose of this study is to examine the efficacy of the active interventions (exercise or wellness/support intervention) compared to usual care on the prevention of postpartum depression among wom...

Detailed Description

The purpose of this study is to examine the efficacy of exercise and wellness/support interventions for preventing postpartum depression. Specifically, 450 sedentary postpartum women (2-6 weeks postpa...

Eligibility Criteria

Inclusion

  • Generally healthy
  • Low active
  • Currently pregnant (who will wait to be randomized until postpartum) or less than six weeks postpartum
  • History of depression

Exclusion

  • Less than 18 years of age
  • Pre-existing hypertension or diabetes
  • Currently exercising (defined as exercising more than 60 minutes per week)
  • Enrolled in another exercise or weight management study
  • Another member of the household participating in the study
  • Unable to exercise for 20 minutes continuously
  • Musculoskeletal problems such as arthritis, gout, osteoporosis, or back, hip or knee pain that may interfere with exercising
  • Exercise induced asthma
  • Any condition that would make exercise unsafe or unwise
  • Taking medication that interferes with heart rate response to exercise such as beta blockers
  • Hospitalization for a psychiatric disorder in the past six months
  • Current depressive episode (based on the SCID) and/or currently receiving antidepressant medication or psychotherapy for depression (participants who are depressed prior to randomization will be referred to their primary physician or psychiatrist)

Key Trial Info

Start Date :

December 1 2012

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

May 1 2017

Estimated Enrollment :

450 Patients enrolled

Trial Details

Trial ID

NCT01883479

Start Date

December 1 2012

End Date

May 1 2017

Last Update

June 29 2017

Active Locations (1)

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1

University of Minnesota

Minneapolis, Minnesota, United States, 55455