Clinical trial Recruiting at 1 site Interventional Ages 18 and up

Essential Coaching Postpartum: a 6-week parent-focused text messaging program in Nova Scotia

Official title: Essential Coaching Postpartum: Evaluating a Parent-focused Postpartum Text Message Program in Nova Scotia

Run by IWK Health Centre · NCT06996067 · Data updated 2026-11-12

This study will test if a 6-week series of supportive, tailored text messages helps first-time birthing and non-birthing parents in Nova Scotia feel more confident and less anxious after their baby is born.

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment332 (estimated)
SponsorIWK Health Centre
Academic / other
Locations1 site (Halifax, Nova Scotia)
StatusRecruiting
StartedJune 5, 2025
Main results expectedDecember 2027
Study endsJune 2028
Registry record updatedJuly 6, 2026
Trial IDNCT06996067 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

First-time birthing and non-birthing parents in Nova Scotia who are 18 or older, English-speaking, within 7 days postpartum, and have a cellphone capable of receiving texts and data.

Probably not a fit

People who cannot receive SMS (no phone or unwilling), who are not English-speaking, who live outside Nova Scotia, or whose newborn has died or is expected to die prior to hospital discharge are excluded and unlikely to benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

Researchers will enroll about 332 first-time birthing and non-birthing parents within 7 days of delivery and deliver tailored text messages for 6 weeks, with separate message streams for birthing parents and non-birthing partners. The messages cover newborn care and parental mental-health topics intended to support parenting self-efficacy and reduce postpartum anxiety, depression, and stress. Participants must be 18 or older, English-speaking, have a cellphone with text and data capability, and live in Nova Scotia; those without phone access or who opt out are excluded. Outcomes will be measured using standardized questionnaires and follow-up contact per the study protocol.

Why it matters

Potential benefit: If successful, the program could increase new parents' confidence and reduce postpartum anxiety, depression, and feelings of isolation by delivering timely information and support via text.

How similar studies have gone: Previous postpartum text-message interventions have shown modest benefits for maternal support and confidence, though partner-targeted programs are less commonly tested.

Who can join: the full rules

Show full inclusion / exclusion criteria
INCLUSION CRITERIA:

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.

EXCLUSION CRITERIA:

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).

Where it's running

  • IWK Health
    Halifax, Nova Scotia, Canada
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.