Using Cueing Interventions to Promote Breastfeeding

Overview

Background: Interventions focusing on promoting good behavioural intentions were found to only have small-to-moderate effect sizes on changing the actual behaviours. Self-regulation plays an important role to maintain individual attentions to the distant benefits of healthy behaviours and resist to proximal tempting cues from unhealthy behaviours, and thereby facilitate the translation of good intention into actual behaviours. However, self-regulation resources are limited and can be depleted in certain contexts. Providing environmental cues relevant to the desirable behaviours can activate the nonconscious process and lead to behavioural change without conscious awareness, the underlying mechanism of cueing interventions. Aims: To test the effectiveness of using two types of cues, social normative and goal-related cues, to activate the nonconscious process for facilitating the translation of intentions into actual behaviours. We hypothesize that (1) cueing interventions will be more effective than will conventional education-based interventions (providing factual information about health benefits) be for changing behaviours; (2) cueing interventions are more effective for participants who have a tendency to use an intuitive mode in information processing; and (3) goal priming is more effective for participants with stronger motivation to pursue the goal of sustaining breastfeeding. Subject and study design: The hypotheses will be tested in the behavioural context of breastfeeding among first-time mothers because: first, primiparous women may have less self-regulation resources due to high cognitive demand for postpartum adjustment during motherhood transition; and second, while breastfeeding intention and initiation were high, maintaining breastfeeding for the first six months postpartum was generally low in Hong Kong, indicating a substantial intention-behaviour gap. We propose to recruit 600 primiparous women. Baseline assessments will be conducted face-to-face using a standardized questionnaire. Participants will be randomly allocated to the control group (receive education-based messages about the health benefit of breastfeeding) or one of the two intervention groups (receive either social normative cues or goal-related cues related to breastfeeding). All messages will be delivered through smartphone on a daily basis over 16 weeks postpartum.

Full Title of Study: “Using Cueing Interventions to Bridge Intention-behaviour Gaps: an Longitudinal Experimental Study on Promoting Breastfeeding”

Study Type

  • Study Type: Interventional
  • Study Design
    • Allocation: Randomized
    • Intervention Model: Parallel Assignment
    • Primary Purpose: Health Services Research
    • Masking: Single (Outcomes Assessor)
  • Study Primary Completion Date: February 6, 2023

Interventions

  • Behavioral: Cue intervention
    • Around 30 pieces of narrative information about how a mother behaves in specific decision context will be derived from our qualitative study to construct social normative cues. For goal-related cues, words relating to each category of breastfeeding-related values, benefits and goals will be identified and used to construct the messages (e.g. “attractive body shape”, “smart baby”, “natural”, “strong immunity” and etc.). Each goal-priming message will be presented with brief priming words and a picture of an image of the desirable goal.

Arms, Groups and Cohorts

  • No Intervention: Control group
    • Receive education-based messages about the health benefit of breastfeeding
  • Other: Social normative cues
    • Receive social normative cues related to breastfeeding
  • Other: Goal-related cues
    • Receive goal-related cues related to breastfeeding

Clinical Trial Outcome Measures

Primary Measures

  • The effectiveness of two cueing interventions, cueing with social norms and goal priming at one month postpartum
    • Time Frame: Immediately after participants complete the questionnaire
    • The name of measurement: exclusive and any breastfeeding duration at one month postpartum Unit of measurement: the duration of breastfeeding
  • The effectiveness of two cueing interventions, cueing with social norms and goal priming at three months postpartum
    • Time Frame: Immediately after participants complete the questionnaire
    • The name of measurement: exclusive and any breastfeeding duration at three months postpartum Unit of measurement: the duration of breastfeeding
  • The effectiveness of two cueing interventions, cueing with social norms and goal priming at six months postpartum
    • Time Frame: Immediately after participants complete the questionnaire
    • The name of measurement: exclusive and any breastfeeding duration at six months postpartum Unit of measurement: the duration of breastfeeding

Participating in This Clinical Trial

Inclusion Criteria

  • being ≥18 years – being Chinese ethnicity and Hong Kong residents – without any serious medical or obstetric complications – having a full-term (i.e. gestational age ≥37 weeks) healthy infant with normal birthweight (≥2,500 grams) Exclusion Criteria:

  • with linguistic and cognitive barriers impeding completion of face-to-face and telephone interviews or comprehension of the intervention materials – physical anomalies that contraindicate breastfeeding

Gender Eligibility: Female

First-time mothers from the postnatal wards

Minimum Age: 18 Years

Maximum Age: N/A

Are Healthy Volunteers Accepted: Accepts Healthy Volunteers

Investigator Details

  • Lead Sponsor
    • The University of Hong Kong
  • Provider of Information About this Clinical Study
    • Principal Investigator: Qiuyan Liao, Assistant Professor – The University of Hong Kong

Clinical trials entries are delivered from the US National Institutes of Health and are not reviewed separately by this site. Please see the identifier information above for retrieving further details from the government database.

At TrialBulletin.com, we keep tabs on over 200,000 clinical trials in the US and abroad, using medical data supplied directly by the US National Institutes of Health. Please see the About and Contact page for details.