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Effects of the Parents of Little Ones® - Baby Version® on Parenting Stress and Mindful Parenting in Postpartum Mothers (PdP-B)

2026年11月6日 更新者:Helena Moreira、University of Coimbra

Efficacy of the Self-Guided Online Parents of Little Ones® - Baby Version® Program in Promoting Mindful Parenting and Reducing Parenting Stress Among Postpartum Mothers: A Randomized Controlled Trial

The goal of this clinical trial is to evaluate whether Parents of Little Ones® - Baby Version®, a self-guided online parenting program, can reduce parenting stress and improve mindful parenting among mothers during the first 12 months after childbirth.

The main questions it aims to answer are:

  • Does participation in the program reduce parenting stress?
  • Does participation in the program improve mindful parenting?
  • Are any improvements in parenting stress and mindful parenting maintained three months after the intervention ends?

Researchers will compare mothers who receive access to the self-guided online program with mothers assigned to a waitlist control group to determine whether the program leads to greater reductions in parenting stress and improvements in mindful parenting, both immediately after the intervention and three months later.

Participants will:

  • Complete online questionnaires at three assessment points: before the intervention (baseline), after the intervention period (post-intervention), and three months after the intervention ends (follow-up). These questionnaires will assess parenting stress, mindful parenting, psychological well-being, and other parenting-related outcomes.
  • Be randomly assigned to either the intervention group or the waitlist control group.
  • If assigned to the intervention group, complete eight self-guided online sessions, preferably one per week, including psychoeducational videos, interactive exercises, mindfulness and self-compassion practices, and activities to apply the strategies in everyday parenting.
  • If assigned to the waitlist control group, continue their usual activities without receiving access to the program during the study period.

研究概览

详细说明

The postpartum period is a time of significant psychological, emotional, and relational adjustment. During the first year after childbirth, mothers may experience increased parenting stress and emotional difficulties, which can affect their psychological well-being and interactions with their infants. Accessible, evidence-based preventive interventions may help mothers navigate these challenges and promote more adaptive parenting practices.

The program was developed in two delivery formats: a therapist-guided group format, delivered through synchronous videoconference sessions, and a self-guided online format, delivered through a digital platform specifically developed for the program. The self-guided format was designed to increase accessibility and flexibility, allowing mothers to engage with the intervention independently, according to their availability and daily routines. Both formats comprise eight sessions, preferably completed weekly. The self-guided online version includes psychoeducational videos, interactive exercises, guided mindfulness and self-compassion practices, and activities designed to encourage the application of the learned strategies in everyday parenting situations.

The present randomized controlled trial aims to evaluate the effectiveness of the self-guided online version of Parents of Little Ones® - Baby Version®, compared with a waitlist control condition. The primary outcomes are parenting stress and mindful parenting. Secondary outcomes include maternal psychological well-being, particularly depressive and anxiety symptoms, self-compassion, parental reflective functioning, and other parenting-related variables.

Assessments will be conducted at three time points: baseline (before the intervention), post-intervention (following the intervention period), and three months after the end of the intervention (follow-up). This design will allow researchers to examine both the immediate effects of the program and the maintenance of these effects over time.

研究类型

介入性

注册 (估计的)

264

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

学习地点

      • Coimbra、葡萄牙、3000
        • Center for Research in Neuropsychology and Cognitive-Behavioral Interventions
        • 接触:
        • 首席研究员:
          • Helena Moreira

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 及以上 (成人、年长者)

接受健康志愿者

是的

有资格学习的性别

女性

描述

Inclusion Criteria:

  • Aged 18 years or older.
  • Within the first 12 months postpartum.
  • Able to read and understand Portuguese.
  • Access to the Internet through a computer, tablet, or smartphone.

Exclusion Criteria:

  • Presence of a diagnosed severe mental disorder that may interfere with participation in a self-guided intervention (e.g., severe depressive or anxiety disorder, schizophrenia, bipolar disorder, or substance use disorder).
  • Recent suicidal or self-harm ideation.
  • Current participation in a structured parenting or psychological intervention with substantially overlapping content.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:预防
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的:Self-guided online version of the Parents of Little Ones - Baby version®

Participants allocated to this arm will receive access to Parents of Little Ones® - Baby Version®, a self-guided online parenting program consisting of eight sessions, preferably completed over eight weeks. The program integrates cognitive-behavioral, mindfulness, self-compassion, and mindful parenting strategies. Sessions include psychoeducational videos, interactive exercises, guided practices, and activities to apply the learned strategies in everyday parenting. Participants will complete online questionnaires at baseline, post-intervention (up to week 10), and three-month follow-up (up to week 22).

Parents of Little Ones® - Baby Version® is a self-guided online preventive parenting program designed for mothers during the first 12 months postpartum. The program integrates cognitive-behavioral strategies, mindfulness, self-compassion, acceptance-based approaches, attachment theory, and mindful parenting principles.

The intervention consists of eight online sessions, each lasting approximately 45 minutes, preferably completed at a weekly pace over eight weeks. Sessions include psychoeducational videos, interactive exercises, guided mindfulness and self-compassion practices, and activities designed to help participants apply the strategies in everyday parenting situations.

Participants access the program independently through an online platform, without therapist guidance. The program aims to reduce parenting stress, promote mindful parenting, strengthen maternal psychological resources, and support positive mother-infant interactions.

无干预:Wait-list control condition

Participants assigned to the waitlist control group will not receive access to the Parents of Little Ones® - Baby Version® program during the study period. They will continue their usual activities and complete online questionnaires at baseline, post-intervention (up to week 10), and three-month follow-up (up to week 22), following the same assessment schedule as the intervention group.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Changes in Parenting Stress From Baseline (week 0) to Post-Intervention (up to week 10) and 3-Month Follow-Up (up to week 22)
大体时间:Baseline (week 0), Post-Intervention (up to week 10) and 3-Month Follow-Up (up to week 22)

Changes in parenting stress will be assessed through Parental Stress Scale (PSS). The questionnaire assesses the distress associated with the parental role and has 18 items (e.g., "Caring for my child(ren) sometimes takes more time and energy than I have to give") answered on a five-point Likert scale that ranges from 1 (strongly disagree) to 5 (strongly agree). The total score is calculated as the sum of the items, with higher scores indicating higher levels of parenting stress.

Baseline (week 0), Post-Intervention (up to week 10) and 3-Month Follow-Up (up to week 22)
Changes in Mindful Parenting From Baseline (week 0) to Post-Intervention (up to week 10) and 3-Month Follow-Up (up to week 22)
大体时间:Baseline (week 0), Post-Intervention (up to week 10) and 3-Month Follow-Up (up to week 22)

Changes in mindful parenting will be measured by the Interpersonal Mindfulness in Parenting Scale - Infant version (IM-P-I), an adapted version of the Portuguese version of the Interpersonal Mindfulness in Parenting Scale for parents of infants. This version consists of 28 items (e.g., "I tend to criticize myself for not being the kind of parent I want to be") rated on a five-point Likert scale from 1 (never true) to 5 (always true). The scale assesses five mindful parenting dimensions: Listening with Full Attention, Emotional Awareness of the Child, Compassion for the Child, Self-Regulation in Parenting, and Nonjudgmental Acceptance of Parental Functioning. The total score, representing a global measure of mindful parenting, is calculated by summing all the item responses, with higher scores indicating higher levels of mindful parenting.

Baseline (week 0), Post-Intervention (up to week 10) and 3-Month Follow-Up (up to week 22)

次要结果测量

结果测量
措施说明
大体时间
Changes in Depression Symptoms From Baseline (week 0) to Post-Intervention (up to week 10) and 3-Month Follow-Up (up to week 22)
大体时间:Baseline (week 0), Post-Intervention (up to week 10) and 3-Month Follow-Up (up to week 22)

The presence of depressive symptomatology will be assessed through the Edinburgh Postnatal Depression Scale (EPDS). The EPDS is a 10-item screening tool designed to measure the presence of depressive symptoms (e.g., sadness, tearfulness) in the previous seven days (e.g., "I have been able to laugh and see the funny side of things"). Items are answered in a four-point Likert scale (from 0 to 3). The total score is calculated by summing all item responses, with higher scores indicating greater levels of depressive symptoms. The EPDS total scores will be interpreted using the following severity ranges: none or minimal depression (0-6), mild depression (7-13), moderate depression (14-18), and severe depression (19-30).

Baseline (week 0), Post-Intervention (up to week 10) and 3-Month Follow-Up (up to week 22)
Changes in Anxiety Symptoms From Baseline (week 0) to Post-Intervention (up to week 10) and 3-Month Follow-Up (up to week 22)
大体时间:Baseline (week 0), Post-Intervention (up to week 10) and 3-Month Follow-Up (up to week 22)

Changes in anxiety will be assessed through the Postpartum Specific Anxiety Scale - Research Short Form (PSAS-RSF). The PSAS-RSF is a 16-item self-report questionnaire derived from the original 51-item PSAS to assess specific anxieties related to the postpartum period. As in the original scale, items are divided into four factors: (1) Maternal Competence and Attachment Anxieties; (2) Infant Safety and Welfare Anxieties; (3) Practical Infant Care Anxieties; and (4) Psychosocial Adjustment to Motherhood. Mothers should answer each item considering how they felt in the last seven days, using a four-point Likert scale ranging from 1 (never) to 4 (almost always). The total and subscale scores consist of the sum of the items, with higher scores indicating higher levels of postpartum specific anxiety.

Baseline (week 0), Post-Intervention (up to week 10) and 3-Month Follow-Up (up to week 22)
Changes in Maternal Confidence From Baseline (week 0) to Post-Intervention (up to week 10) and 3-Month Follow-Up (up to week 22)
大体时间:Baseline (week 0), Post-Intervention (up to week 10) and 3-Month Follow-Up (up to week 22)

The Maternal Confidence Questionnaire (MCQ) will be used to measure changes in maternal confidence. The MCQ is an instrument that measures a mother's perceived competence in caring for her infant and understanding their needs. It has 13 items (e.g., "I know what makes my baby happy") answered using a five-point Likert scale, ranging from 1 (never) to 5 (always) with higher scores indicating higher maternal perceived competence.

Baseline (week 0), Post-Intervention (up to week 10) and 3-Month Follow-Up (up to week 22)
Changes in Mother-Infant Bond From Baseline (week 0) to Post-Intervention (up to week 10) and 3-Month Follow-Up (up to week 22)
大体时间:Baseline (week 0), Post-Intervention (up to week 10) and 3-Month Follow-Up (up to week 22)

The mother-infant bonding will be assessed by the Postpartum Bonding Questionnaire (PBQ). The PBQ is a self-report questionnaire designed to provide an early indication of mother-infant bonding disorders. It has 12 items (e.g., "I feel distant from my baby") to be rated on a six-point Likert scale, ranging between 0 (never) and 5 (always). The total score is calculated as the sum of the items, with higher scores indicating more impaired mother-infant bonding.

Baseline (week 0), Post-Intervention (up to week 10) and 3-Month Follow-Up (up to week 22)
Changes in Coparenting From Baseline (week 0) to Post-Intervention (up to week 10) and 3-Month Follow-Up (up to week 22)
大体时间:Baseline (week 0), Post-Intervention (up to week 10) and 3-Month Follow-Up (up to week 22)

The Perceptions of Coparenting Partners Questionnaire (PCPQ) will be used to assess changes in the coparenting relationship. PCPQ is a self-report questionnaire designed to assess parents' perceptions of the quality of their coparenting relationship. The questionnaire includes 14 items that assess supportive coparenting behaviors (e.g., "My partner and I use similar parenting strategies") and non-supportive coparenting behaviors (e.g., "My partner uses parenting strategies that I asked him or her not to use"). Items are rated on a five-point Likert scale ranging from 1 (never) to 5 (always), and the total score is obtained by calculating the average of all item scores after reversing the scores for non-supportive coparenting behaviors. A higher total score indicates a greater level of supportive coparenting.

Baseline (week 0), Post-Intervention (up to week 10) and 3-Month Follow-Up (up to week 22)
Changes in Baby Social-Emotional and Behavioral Development From Baseline (week 0) to Post-Intervention (up to week 10) and 3-Month Follow-Up (up to week 22)
大体时间:Baseline (week 0), Post-Intervention (up to week 10) and 3-Month Follow-Up (up to week 22)

Changes in baby social-emotional and behavioral development will be assessed by the Baby Pediatric Symptom Checklist (BPSC). The BPSC is a caregiver-reported screening tool designed to identify difficulties in infants. The measure includes 12 items organized into three domains: Irritability, Inflexibility, and Difficulty with Routines. Each domain comprises four items rated on a three-point scale from 0 (not at all) to 2 (very much). The instrument is intended to facilitate the early detection of potential social and emotional concerns in very young children, supporting timely follow-up when needed. A score of 3 or higher on any subscale suggests that the child may be at risk and warrants further evaluation or clinical attention.

Baseline (week 0), Post-Intervention (up to week 10) and 3-Month Follow-Up (up to week 22)
Changes in Mindfulness From Baseline (week 0) to Post-Intervention (up to week 10) and 3-Month Follow-Up (up to week 22)
大体时间:Baseline (week 0), Post-Intervention (up to week 10) and 3-Month Follow-Up (up to week 22)

Levels of dispositional mindfulness will be measured by the Mindful Attention Awareness Scale (MAAS). The MAAS comprises 15 items (e.g., "I find it difficult to stay focused on what is happening in the present moment"), rated on a six-point Likert scale ranging from 1 (Almost always) to 6 (Almost never). This instrument assesses an unidimensional construct, reflecting aspects related to a receptive state of mind in which attention is guided by an aware sensitivity to present-moment experiences, involving the simple observation of ongoing events as they unfold. A total scale score may be obtained by summing all items, with higher scores indicating greater levels of dispositional mindfulness.

Baseline (week 0), Post-Intervention (up to week 10) and 3-Month Follow-Up (up to week 22)
Changes in Self-Compassion From Baseline (week 0) to Post-Intervention (up to week 10) and 3-Month Follow-Up (up to week 22)
大体时间:Baseline (week 0), Post-Intervention (up to week 10) and 3-Month Follow-Up (up to week 22)

The Self-Compassion Scale - Short Form (SCS-SF) will be used to assess parents' levels of self-compassion. This scale includes 12 items (e.g., "I try to be understanding and patient toward those aspects of my personality I don't like") that are rated on a five-point Likert scale, from 1 (almost never) to 5 (almost always). The overall score is calculated as the mean of the items, with higher scores reflecting greater self-compassion.

Baseline (week 0), Post-Intervention (up to week 10) and 3-Month Follow-Up (up to week 22)
Changes in Parental Reflective Functioning From Baseline (week 0) to Post-Intervention (up to week 10) and 3-Month Follow-Up (up to week 22)
大体时间:Baseline (week 0), Post-Intervention (up to week 10) and 3-Month Follow-Up (up to week 22)

The Parental Reflective Functioning Questionnaire (PRFQ) will be used to assess parents' levels of reflective functioning. The PRFQ is a multidimensional self-report measure consisting of 18 items scored on a seven-point Likert scale ranging from 1 (strongly disagree) to 7 (strongly agree). The instrument includes three subscales: (a) Pre-Mentalizing Modes of Mental States, with higher scores indicating greater difficulty with understanding and interpreting a child's mental experience; (b) Certainty about Mental States, with higher scores reflecting more certainty about what a child is thinking, feeling, or intends to do; and (c) Interest and Curiosity in Mental States, with higher scores reflecting a higher level of parents' interest in their children's inner experiences.

Baseline (week 0), Post-Intervention (up to week 10) and 3-Month Follow-Up (up to week 22)

其他结果措施

结果测量
措施说明
大体时间
Resource utilization
大体时间:Baseline (week 0), Post-Intervention (up to week 10)

Participants' resource utilization will be assessed retrospectively through a Resource Use Questionnaire developed by the research team based on previously published instruments. The questionnaire will collect information regarding resource utilization for both participants and their children, including healthcare utilization (e.g., emergency department visits, outpatient appointments, hospitalizations, and medication use), absenteeism and presenteeism related to paid and unpaid work among caregivers, and out-of-pocket expenses.

Baseline (week 0), Post-Intervention (up to week 10)
Feasibility of the Intervention
大体时间:Post-treatment (up to week 10)

Program feasibility will be evaluated using indicators of adherence, engagement, and attrition. Adherence will be assessed based on the number of sessions completed and the proportion of participants who complete the intervention. Intervention completers will be defined as participants who complete at least 75% of the program. Engagement with the intervention will be examined using platform usage data. Intervention attrition will be assessed based on the proportion of participants who fail to meet the intervention completion criterion within 10 weeks of randomization and will therefore be considered intervention dropouts.

Post-treatment (up to week 10)
Acceptability of the Intervention
大体时间:Post-treatment (up to week 10)

Intervention acceptability will be assessed using study-specific items developed by the research team to capture participants' experiences and perceptions of the program. At the end of the intervention, participants will complete a Final Evaluation Form assessing overall satisfaction with the program, perceived usefulness and impact on parenting, and willingness to recommend the program to others. The form will also assess the usability of the online platform (e.g., ease of use and navigation, clarity of instructions, and comfort using the platform), perceived fit of the intervention with participants' daily routines, perceptions of the intervention format (e.g., session length and overall program duration), and perceived adequacy of contact with the research team. Open-ended questions will invite participants to identify the aspects of the program they found most and least helpful and to provide suggestions for improvement.

Post-treatment (up to week 10)

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:Helena Moreira, PhD、University of Coimbra, Faculty of Psychology and Educational Sciences

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (估计的)

2027年1月1日

初级完成 (估计的)

2027年10月1日

研究完成 (估计的)

2027年10月1日

研究注册日期

首次提交

2026年10月29日

首先提交符合 QC 标准的

2026年11月6日

首次发布 (实际的)

2026年11月12日

研究记录更新

最后更新发布 (实际的)

2026年11月12日

上次提交的符合 QC 标准的更新

2026年11月6日

最后验证

2026年11月1日

更多信息

与本研究相关的术语

其他研究编号

  • FCG/Growing Minds947181
  • FCG/Growing Minds 947181 (其他赠款/资助编号:Fundação Calouste Gulbenkian)

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

IPD 计划说明

Individual participant data will not be made publicly available due to participant confidentiality, privacy considerations, and compliance with the General Data Protection Regulation (GDPR). Study findings will be disseminated through scientific publications and conference presentations, using aggregated and anonymized results.

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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