NCT06996067

Brief Summary

The transition to parenthood is often an exciting yet hard period for parents. In the first year after a new baby, many parents feel less confident, have more anxiety and depression, and feel more isolated and alone. During this time, many parents use their phones and the Internet to seek out information and support. Thus, the investigators are exploring the opportunity of using mHealth, or mobile health, to provide information directly to parents after the birth of their first baby. The investigators have developed a program for both birthing and non-birthing parents called the Essential Coaching Postpartum program. This program provides 332 parents with text messages sent for 6 weeks after birth to share information on newborn care and parent outcomes. This will be tailored based on whether they are the birthing parent (Essential Coaching for Every Mother) or non-birthing parent (Essential Coaching for Every Partner). The investigators will evaluate this program by comparing a group of parents who receive the messages to a group of parents do not receive any text messages. To determine the success of the Essential Coaching Postpartum program, the investigators will compare parents' confidence, anxiety, depression, and co-parenting between the two groups after six-weeks and six-months. The investigators believe that parents who get the text messages will have higher confidence and co-parenting outcomes and lower anxiety and depression. The investigator's goal with the Essential Coaching Postpartum program is to help make the first few weeks after a new baby less stressful by providing information and support directly to parents that they know they can trust.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
332

participants targeted

Target at P75+ for not_applicable

Timeline
13mo left

Started Jun 2025

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress46%
Jun 2025Jun 2027

First Submitted

Initial submission to the registry

May 21, 2025

Completed
9 days until next milestone

First Posted

Study publicly available on registry

May 30, 2025

Completed
6 days until next milestone

Study Start

First participant enrolled

June 5, 2025

Completed
1.5 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2026

Expected
6 months until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2027

Last Updated

March 27, 2026

Status Verified

March 1, 2026

Enrollment Period

1.5 years

First QC Date

May 21, 2025

Last Update Submit

March 24, 2026

Conditions

Keywords

text messagingnon-birthing parentbirthing parentsmothersfathersdigital health

Outcome Measures

Primary Outcomes (1)

  • Parenting self-efficacy

    Parenting self-efficacy will be measured using the Karitane Parenting Confidence Scale (KPCS) tool. This 15-item tool was developed to assess perceived self-efficacy of parents of infants birth to twelve months of age and has acceptable internal consistent (Cronbach's alpha = 0.81) and test-retest reliability (r = 0.88). A cut off score of 39 or less (out of a possible 45) was determine to be a clinically low perceived parenting self-efficacy (PPSE).

    Enrollment, 6-weeks postpartum, 6-months postpartum

Secondary Outcomes (7)

  • Postnatal Anxiety

    Enrollment, 6-weeks postpartum, 6-months postpartum

  • Postpartum depression

    Enrollment, 6-weeks postpartum, 6-months postpartum

  • Postnatal Childcare Stress

    Enrollment, 6-weeks postpartum, 6-months postpartum

  • General distress

    Enrollment, 6-weeks postpartum, 6-months postpartum

  • Sleep

    Enrollment, 6-weeks postpartum, 6-months postpartum

  • +2 more secondary outcomes

Study Arms (2)

Essential Coaching Postpartum

EXPERIMENTAL
Behavioral: Essential Coaching Postpartum

Standard care

NO INTERVENTION

Interventions

Essential Coaching Postpartum consists of one-way, standardized text messages sent to parents from birth to 6-weeks postpartum to provide evidence-based information on newborn care and mental health. Messages are sent twice a day for the first three weeks (10am and 5pm) and then once a day for the following three weeks (10am), starting the second day after birth.

Also known as: Essential Coaching for Every Mother, Essential Coaching for Every Partner
Essential Coaching Postpartum

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Eligible birthing parents will
  • early postpartum (\<7 days) with their first child
  • understand English
  • have a cell phone with text and data
  • be 18 years of age or old
  • live in Nova Scotia.
  • Eligible non-birthing parents will:
  • be early postpartum (\<7 days) with their first child
  • understand English
  • have a cell phone with text and data
  • be 18 years of age or old
  • live in Nova Scotia.

You may not qualify if:

  • Participants (both birthing and non-birthing parents) will be excluded if:
  • newborn die or are expected to die prior to leaving the hospital
  • they have no access to mobile phone, either personal or shared
  • unwilling to receive SMS messages
  • decline or withdraw to participate
  • participated in a previous iteration of this project (e.g., either the development or evaluation).

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

IWK Health

Halifax, Nova Scotia, Canada

RECRUITING

Related Publications (1)

  • Dol J, Chambers CT, Parker JA, Brooks M, Dennis CL, Seguin D, Goldberg JM, Hughes B, Reese T, Richard G, Calnan K. Effectiveness of the Essential Coaching Postpartum Digital Health Solution on Parenting Self-Efficacy, Mental Health, Well-Being, and Parenting Outcomes: Protocol for a Randomized Controlled Trial. JMIR Res Protoc. 2025 Oct 17;14:e78209. doi: 10.2196/78209.

    PMID: 41105940BACKGROUND

MeSH Terms

Conditions

Depression, PostpartumPsychological Well-Being

Condition Hierarchy (Ancestors)

Puerperal DisordersPregnancy ComplicationsFemale Urogenital Diseases and Pregnancy ComplicationsUrogenital DiseasesDepressive DisorderMood DisordersMental DisordersPersonal SatisfactionBehavior

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
CARE PROVIDER
Purpose
PREVENTION
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Accelerate Chair in Women+ Health Research (Principal Investigator)

Study Record Dates

First Submitted

May 21, 2025

First Posted

May 30, 2025

Study Start

June 5, 2025

Primary Completion (Estimated)

December 1, 2026

Study Completion (Estimated)

June 1, 2027

Last Updated

March 27, 2026

Record last verified: 2026-03

Data Sharing

IPD Sharing
Will not share

Locations