此页面是自动翻译的,不保证翻译的准确性。请参阅 英文版 对于源文本。

Feasibility and Acceptability of a Novel Digital Intervention For Perinatal Men Who Have Depression or Anxiety (TIP-PLUS)

2026年8月4日 更新者:Women and Infants Hospital of Rhode Island

Pilot Randomized Trial of Together in Parenting, a Novel Digital Paternal Mental Health Intervention, For Fathers With Anxiety or Depression

Postpartum depression (PPD) occurs almost as often among men as it does among women. However, while there have been multiple programs designed to prevent maternal PPD, few, if any, interventions exist that have been created specifically to prevent paternal PPD. After engaging in evidence-based qualitative research with soon-to-be or new fathers, a novel interpersonal-therapy based digital program was created to prevent paternal PPD called Together in Parenting (TIP), which comprises multiple podcasts and digital educational handouts. While screening for eligibility for an ongoing pilot feasibility trial (NCT07594743), 20% of those were ineligible because they either endorsed having depression or anxiety or screened positive on psychometric surveys for having moderate symptoms of these conditions. TThe proposed pilot study will examine the feasibility and acceptability of using TIP as an intervention for fathers who have mental health symptoms, and will generate preliminary estimates of effect of the intervention to support a future efficacy study.

研究概览

详细说明

Postpartum depression (PPD) PPD affects 8-10% of men, and paternal anxiety affects up to 15% of men. Paternal mental health symptoms are often underdiagnosed and undertreated. It is hard to identify fathers who have mental health symptoms due to cultural conceptions of masculinity, leading to the risk that fathers do not recognize their symptoms as mental health symptoms and engage in avoidant or numbing behavior instead of appropriate treatment. Even if they recognize their mental health symptoms, men are less likely than women to pursue help due to the stigma of mental health care, resulting in delays in diagnosis and treatment. Fathers' lack of awareness and aversion to treatment leads to untreated PPD, which drastically increases risk of PPD for mothers and impaired cognitive development for children. Given the barriers fathers face being diagnosed with PPD and the lack of tailored treatment, a targeted intervention for fathers that effectively treats mental health symptoms and prevents worsening of these symptoms is urgently needed to decrease the risk of profound intergenerational consequences for fathers, mothers, and infants.

Interpersonal therapy (IPT) is an evidence-based psychotherapy approach for depression that views relationship attachments, effective communication, and disruption in social support as intimately linked with psychological symptoms. In 2019, the USPSTF's maternal PPD statement indicated IPT prevents maternal PPD. IPT may be even more suitable for paternal PPD prevention: fathers have been shown to prefer psychology over pharmacotherapy for PPD. In fact, IPT-based counseling has mechanistic plausibility to prevent paternal PPD: by helping fathers improve communication within their relationships, change expectations about those relationships, and/or build or better utilize an extended social support network, IPT can help fathers develop the interpersonal support needed to deal with the crises precipitating depressive symptoms (birth or infant care). It is also important to note that IPT has been shown to be an effective treatment for both anxiety and depression.

Online interventions reduce the stigma associated with mental health care, are widely utilized by men, and reduce depressive symptoms. Online peripartum mental health care effectively prevents and treats maternal PPD. Though there are currently no ongoing studies examining the effect of online IPT for paternal PPD prevention or treatment, online IPT will be accessible to most fathers: In the US, 90% of adults own a smartphone and 80% have home broadband internet. Also, unlike current IPT-based maternal mental health interventions, which require trained providers for intervention fidelity, online IPT could be disseminated without impacting intervention fidelity.

Together in Parenting (TIP) is a novel online paternal postpartum intervention that utilizes interpersonal-therapy-based strategies to reduce interparental conflicts and increase social support in the newborn period, thereby improve mental health symptoms among fathers. An iterative end-user centered design process allowed qualitative interviews with 25 fathers at high-risk of paternal PPD-as defined by the fact that their partners attended prenatal care at the clinic for federally insured pregnant people-to transform TIP's appearance and features. Specifically, TIP was originally conceptualized as a smartphone application but has evolved iteratively from feedback from target end-users during the qualitative interviews to become a scripted audio- and video-recorded podcast, mimicking friends casually discussing parenting and relationships. Each of the 12 podcasts, referred to as lessons on the website, range between 8 to 15 minutes (most are less than 11 minutes) and include a digital handout to encourage participant engagement with the progressive IPT-based curriculum. There are also 10 digital handouts to encourage engagement. TIP is hosted on a password-protected website. User-specific log-ins allow TIP to contain an embedded analytic platform to monitor duration of use and modules accessed as well as responses to digital handouts.

Thus, a pilot feasibility study is being conducted that examines the feasibility, acceptability, and preliminary estimates of effects of TIP as a paternal mental health program when compared to routine care (NCT07594743). During screening for eligibility, 20% of those screened cannot participate in this trial because they either endorse having depression or anxiety or screen positive for symptoms of depression or anxiety on baseline psychometric surveys. Given IPT can be used to treat these mental health symptoms, a second small feasibility and acceptability study is now being proposed to examine whether TIP can improve mental health symptoms among fathers with depression or anxiety.

For this pilot study, the primary purpose will not be to determine TIP's efficacy at improving paternal mental health symptoms but to demonstrate the feasibility and acceptability of TIP as a digital intervention among fathers with newly born infants and who have mental health symptoms. The dual primary outcome for this study will be feasibility and acceptability. In order to obtain a preliminary estimate of effect for TIP on PPD outcomes to support a future efficacy trial, the proposed pilot study will also assess clinically meaningful perinatal mental health outcomes (depression and anxiety) and mediators (dyadic adjustment, stress, loneliness, and parenting confidence). These metrics will be collected at multiple time points after randomization to allow for longitudinal assessment of symptom trajectories postpartum as well as pre/post-intervention analyses comparing scores at randomization to those at various postpartum intervals. The effect of TIP on maternal well-being will be examined by having mothers complete some psychometric at study completion. Lastly, the most effective timing of intervention delivery will be determined using a mixed-methods approach nested within the proposed pilot randomized trial.

研究类型

介入性

注册 (估计的)

45

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

  • 姓名:Stephanie Nunes, MS
  • 电话号码:401-274-1122
  • 邮箱:snunez@wihri.org

学习地点

    • Rhode Island
      • Providence、Rhode Island、美国、02903
        • Women & Infants Hospital of Rhode Island

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

  • 成人
  • 年长者

接受健康志愿者

不

描述

Inclusion Criteria:

  1. English-speaking (for now, TIP is only available in English)
  2. age >18 years old,
  3. smartphone ownership or access to home internet,
  4. partner or patient received or receiving prenatal care from a resident or nurse-practitioner/midwifery clinic at the Obstetrics and Gynecologic Care Center (OGCC) at Women & Infants Hospital of Rhode Island (WIHRI) or receiving an ultrasound at the WIHRI's Prenatal Diagnosis Center ,
  5. planned delivery or status post delivery at WIHRI.
  6. self-reported history of depression/anxiety or active depression/anxiety or screen positive on GAD-7 (8 or higher) or MDS (13 or higher)

Exclusion Criteria:

  1. Endorsing active suicidality on intake survey;
  2. prisoners;
  3. infant with genetic abnormality, significant anatomic malformation, or NICU admission at time of enrollment;
  4. inability to consent.

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:治疗
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:三倍

武器和干预

参与者组/臂
干预/治疗
实验性的:Together in Parenting (intervention)
Password protected website that contains digital intervention, Together in Parenting (TIP). TIP delivers a progressive interpersonal therapy-based curriculum through a podcast format with interactive handouts.
Together in Parenting is an novel digital intervention that was designed specifically to improve paternal mental health symptoms and was optimized via qualitative research with target end-users. The interpersonal therapy-based program contains four modules that include content on infant care and parenting education and a progressive, interactive interpersonal therapy-based curriculum. Each module contains four audio- and video-record podcasts that last 8-15 minutes, with most less than 10 minutes. In addition, TIP contains voluntary exercises to engage users with specific content after some podcast (there are 10 exercises in total). Those who complete all four modules and all will receive a digital certificate of completion.
无干预:Treatment As Usual (routine care)
Routine care will be provided to those randomized to this 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
Feasibility of Together in Parenting as a paternal mental health intervention
大体时间:From randomization until 3 months postpartum
Percentage of participants who view at least 6 of the 12 audio and video podcasts
From randomization until 3 months postpartum
Acceptability of Together in Parenting as paternal mental health intervention
大体时间:3 months postpartum
Client Satisfaction Questionnaire (8 item survey assessing satisfaction; scores range from 8-32 with higher scores indicating greater satisfaction)
3 months postpartum

次要结果测量

结果测量
措施说明
大体时间
Feasibility: recruitment
大体时间:Prior to randomization
Percentage of participants who approached to participate who consent
Prior to randomization
Acceptability: System Usability Scale
大体时间:3 months postpartum
8-item survey measuring perceived usability of digital products (score 0-100, with score >68 reflecting above average usability)
3 months postpartum
Paternal postpartum depressive symptoms
大体时间:Six or twelve weeks postpartum
Masculine Depressive Scale: 13-item score designed specifically for men to assess symptoms of depression. The score ranges from 0-39 and screening positive is a score of 13 or higher
Six or twelve weeks postpartum
Paternal postpartum anxiety symptoms
大体时间:Six or twelve weeks postpartum
Generalized anxiety disorder-7: 7-item self-reported anxiety symptoms. The score range from 0-21, with higher scores indicating greater severity
Six or twelve weeks postpartum
Paternal postpartum perceived stress
大体时间:Six or twelve weeks postpartum
Perceived Stress Scale-4: 4-item self-report on stress symptoms. The score range is 0-16, with higher scores denoting higher stress.
Six or twelve weeks postpartum
Paternal positive screens for mood disorders
大体时间:Six or twelve weeks postpartum
Paternal screening positive for postpartum depression or anxiety (i.e,, masculine depression score of 13 or higher and/or generalized anxiety disorder-7 score of 10 or higher)
Six or twelve weeks postpartum
Maternal postpartum stress
大体时间:12 weeks postpartum
Maternal scores on the perceived Stress Scale-4: 4-item self-report on stress symptoms. The score range is 0-16, with higher scores denoting higher stress
12 weeks postpartum

其他结果措施

结果测量
措施说明
大体时间
Maternal parenting self-confidence
大体时间:3 months postpartum
Maternal scores on Parenting Sense of Self-Confidence-Revised score: 16-item survey assessing parenting competence and satisfaction. The score range is 16-96, with higher scores (especially 74 or higher) suggesting high competence and satisfaction.
3 months postpartum
Qualitative
大体时间:3 months postpartum
One-on-one interviews with cohort of those randomized to intervention about their user experience and the program's strengths and limitations
3 months postpartum
Paternal dyadic adjustment
大体时间:Six or twelve weeks postpartum
Paternal scores on Dyadic Adjustment Scale, a 7-time survey measuring relationship satisfaction, decision-making, and cohesion. Scores range from 0-35, with higher scores indicating higher adjustment
Six or twelve weeks postpartum
Paternal parenting self-confidence
大体时间:12 weeks postpartum
Paternal scores on Parenting Sense of Self-Confidence-Revised score: 16-item survey assessing parenting competence and satisfaction. The score range is 16-96, with higher scores (especially 74 or higher) suggesting high competence and satisfaction.
12 weeks postpartum
Paternal loneliness
大体时间:Six or twelve weeks postpartum
Paternal scores on UCLA Loneliness Scale, a 20-item survey measuring loneliness. The score range is 20-80, with higher scores indicating greater loneliness
Six or twelve weeks postpartum
New paternal diagnosis of psychiatric condition
大体时间:From randomization until three months postpartum
Initiation of antidepressant or other psychotropic medication during study period by the father
From randomization until three months postpartum
Maternal dyadic adjustment
大体时间:Three months postpartum
Maternal scores on Dyadic Adjustment Scale, a 7-time survey measuring relationship satisfaction, decision-making, and cohesion. Scores range from 0-35, with higher scores indicating higher adjustment
Three months postpartum

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。

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)

2026年9月1日

初级完成 (估计的)

2026年12月31日

研究完成 (估计的)

2027年6月1日

研究注册日期

首次提交

2026年7月28日

首先提交符合 QC 标准的

2026年7月28日

首次发布 (实际的)

2026年8月3日

研究记录更新

最后更新发布 (实际的)

2026年8月7日

上次提交的符合 QC 标准的更新

2026年8月4日

最后验证

2026年7月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

是的

IPD 计划说明

After the primary study is published, IPD that has been deidentified will be shared with any investigator who is interested and contacts the study PI

IPD 共享时间框架

For three years after publication of primary manuscript

IPD 共享访问标准

Any investigator who desires the above IPD and supporting information can contact the study team and engage with the study PI, who will facilitate data transfer as word documents, excel files, or STATA databases as indicated.

IPD 共享支持信息类型

  • 研究方案
  • 树液
  • 国际碳纤维联合会
  • 分析代码

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.

订阅