Mom: Managing Our Mood, Part of The Family Help Program

Postpartum Depression Clinical Trial

— MOM  

Official title:

Evidence-based, Distance Treatment for Postpartum Depression, Mom: Managing Our Mood, Part of The Family Help Program

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00795652
• Other study ID #: 3556
• Status: Completed
• Phase: Phase 2
• First received: November 19, 2008
• Last updated: September 1, 2016
• Start date: May 2006
• Est. completion date: February 2010

Study information

• Verified date: September 2016
• Source: IWK Health Centre
• Contact: n/a
• Is FDA regulated: No
• Health authority: Canada: Canadian Institutes of Health Research
• Study type: Interventional

Clinical Trial Summary

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.

Description:

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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 62
• Est. completion date: February 2010
• Est. primary completion date: February 2010
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Female
• Age group: 19 Years and older

Eligibility

Inclusion Criteria:

• Completed diagnostic measure (SCID), reviewed and signed off by a psychologist

• Participant must meet DSM-IV criteria for postpartum depression

• Significant depressive symptoms that have been present for at least 2 weeks

• Participant must be within 1-12 months postpartum

• Participant must have ready private access to a telephone

• Participant must be between 19-45 years old

• Participant has provided verbal telephone consent

• Participants must speak, read and write in English

• If they are taking medication they must be stabilized (have been on the medication for at least four weeks).

Exclusion Criteria:

• Any condition that in the judgment of the psychologist may interfere with effective delivery of the treatment program (ie, Severe symptomology, challenging diagnostic dilemmas, families who are unmotivated or are in complete chaos)

• Current reports of specific suicidal intentions

• Actively suicidal; suicidal attempts in the previous 6 months

• Participants who are not willing to commit to the demands of treatment

• Participants who have had psychological treatment in the past 6 months for similar problems.

• Participants who have a history of psychotic disorders

• Participants who are cognitively impaired

• Participants who are involved with child protection services

• Participants who have significant substance dependency

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Depression
• Depression, Postpartum
• Depressive Disorder
• Postpartum Depression

Intervention

Behavioral:
• Distance Treatment for postpartum depression
Evidence-based, cognitive behavioural intervention for women with postpartum depression

Locations

Country	Name	City	State
Canada	IWK Health Centre	Halifax	Nova Scotia

Sponsors (2)

Lead Sponsor	Collaborator
IWK Health Centre	Canadian Institutes of Health Research (CIHR)

Country where clinical trial is conducted

Canada, 

References & Publications (5)

Lingely-Pottie P, McGrath PJ. A therapeutic alliance can exist without face-to-face contact. J Telemed Telecare. 2006;12(8):396-9. — View Citation

Lingley-Pottie P, McGrath PJ. A paediatric therapeutic alliance occurs with distance intervention. J Telemed Telecare. 2008;14(5):236-40. doi: 10.1258/jtt.2008.080101. — View Citation

Lingley-Pottie P, McGrath PJ. Distance therapeutic alliance: the participant's experience. ANS Adv Nurs Sci. 2007 Oct-Dec;30(4):353-66. — View Citation

Lingley-Pottie P, McGrath PJ. Telehealth: a child and family-friendly approach to mental health-care reform. J Telemed Telecare. 2008;14(5):225-6. doi: 10.1258/jtt.2008.008001. Review. — View Citation

McGrath PJ, Lingley-Pottie P, Emberly DJ, Thurston C, McLean C. Integrated knowledge translation in mental health: family help as an example. J Can Acad Child Adolesc Psychiatry. 2009 Feb;18(1):30-7. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Diagnosis with SCID (Semi-structured diagnostic interview)		baseline, 120, 240, 365	No
Secondary	Edinburgh Postnatal Depression Scale		baseline, 120, 240, 365	No
Secondary	Sheehan Disability Scale		Baseline, 120, 240, 365	No
Secondary	Satisfaction measure, designed by the investigator		end of intervention	No
Secondary	Beck Depression Inventory-II		baseline, 120, 240 and 365 day follow-up	No