IWK Health Centre
Halifax, Nova Scotia, B3K 6R8, Canada
NCT Number: NCT00795652
The purpose of the MOM: Managing Our Mood Program (part of Family Help) is to evaluate the effectiveness of the Family Help distance intervention compared to usual or standard care typically provided to women with mild to moderate postpartum depression symptomology. This is a single-center trial based at the IWK Health Center. The primary outcome is change in postpartum depression diagnosis.
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Notify Me19 year and older
Female
Interventional
Phase 2
Halifax, Nova Scotia, B3K 6R8, Canada
The Family Help- MOM: Managing Our Mood Program is to deliver, primary care mental health services to mothers in the comfort and privacy of their own home. The purpose of this randomized control trial is to test the effectiveness of the Managing Our Mood (MOM) postpartum depression distance treatment program. This study is a single-centre trial based at the IWK Health Centre, similar to other Family Help Modules.
The goal of this study is to determine the effectiveness of the MOM cognitive-behavioural intervention as an alternative treatment for women suffering from postpartum depression. The intervention is delivered at a distance, using educational materials (handbooks, video-tapes/DVDs, and telephone consultation with a trained paraprofessional coach. Family Help coaches deliver consistent care based on written protocols, with on-going evaluation by a professional team. MOM is not designed to replace specialist care of complex multi-problem mothers.
Eligible participants will be randomly assigned to either active MOM treatment or to the Best Efforts control condition. Those participants assigned to Best Efforts receive printed information about postpartum depression that describes the illness, how it is caused and various treatment options; they are assigned a Coach who books their assessments and is available to answer any questions; they are encouraged to maintain contact and regular care with their family physician or public health nurse for both themselves and their baby. At the end of the 12-month follow-up (one year from randomization), these women will be offered the opportunity to take part in the MOM treatment if they are still depressed.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Evidence-based, cognitive behavioural intervention for women with postpartum depression
Other names: Family Help Program (listed below: other Modules registered), Pediatric Anxiety (2234a) NCT00267566, Pediatric Disruptive Behaviour (2234b) NCT00267579, Pediatric ADHD NCT00267605, Pediatric Recurrent Headache/abdominal Pain NCT00267618, Pediatric Enuresis NCT00270621, Pediatric Sleep Disorder NCT00338429
Time frame: baseline, 120, 240, 365
Time frame: baseline, 120, 240, 365
Time frame: Baseline, 120, 240, 365
Time frame: end of intervention
Time frame: baseline, 120, 240 and 365 day follow-up
IWK Health Centre
Other
Evidence-based, Distance Treatment for Postpartum Depression, Mom: Managing Our Mood, Part of The Family Help Program
Acronym: MOM
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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