Feasibility and Acceptability of a Novel Digital Intervention For Perinatal Men Who Have Depression or Anxiety (TIP-PLUS)
Pilot Randomized Trial of Together in Parenting, a Novel Digital Paternal Mental Health Intervention, For Fathers With Anxiety or Depression
Studieoversigt
Status
Status
Betingelser
Betingelser
Intervention / Behandling
Intervention / Behandling
Detaljeret beskrivelse
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.
Undersøgelsestype
Undersøgelsestype
Tilmelding (Anslået)
Tilmelding
Fase
Fase
- Ikke anvendelig
Kontakter og lokationer
Studiekontakt
Studiekontakt
- Navn: Stephanie Nunes, MS
- Telefonnummer: 401-274-1122
- E-mail: snunez@wihri.org
Studiesteder
-
-
Rhode Island
-
Providence, Rhode Island, Forenede Stater, 02903
- Women & Infants Hospital of Rhode Island
-
-
Deltagelseskriterier
Berettigelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
- Voksen
- Ældre voksen
Tager imod sunde frivillige
Beskrivelse
Inclusion Criteria:
- English-speaking (for now, TIP is only available in English)
- age >18 years old,
- smartphone ownership or access to home internet,
- 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 ,
- planned delivery or status post delivery at WIHRI.
- 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:
- Endorsing active suicidality on intake survey;
- prisoners;
- infant with genetic abnormality, significant anatomic malformation, or NICU admission at time of enrollment;
- inability to consent.
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Tredobbelt
Antal våben
Våben og indgreb
Deltagergruppe / ArmDeltagergruppe / Arm |
Intervention / BehandlingIntervention / Behandling |
|---|---|
|
Eksperimentel: 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.
|
|
Ingen indgriben: Treatment As Usual (routine care)
Routine care will be provided to those randomized to this group
|
Hvad måler undersøgelsen?
Primære resultatmål
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Feasibility of Together in Parenting as a paternal mental health intervention
Tidsramme: 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
Tidsramme: 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
|
Sekundære resultatmål
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Feasibility: recruitment
Tidsramme: Prior to randomization
|
Percentage of participants who approached to participate who consent
|
Prior to randomization
|
|
Acceptability: System Usability Scale
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
|
Andre resultatmål
Andre resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Maternal parenting self-confidence
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
|
Samarbejdspartnere og efterforskere
Sponsor
Sponsor
Datoer for undersøgelser
Studer store datoer
Studiestart (Anslået)
Studiestart
Primær færdiggørelse (Anslået)
Primær færdiggørelse
Studieafslutning (Anslået)
Studieafslutning
Datoer for studieregistrering
Først indsendt
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Først opslået
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering sendt
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Andre undersøgelses-id-numre
Andre undersøgelses-id-numre
- 2277329-1
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
IPD-planbeskrivelse
IPD-delingstidsramme
IPD-delingsadgangskriterier
IPD-deling Understøttende informationstype
- STUDY_PROTOCOL
- SAP
- ICF
- ANALYTIC_CODE
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Studerer et amerikansk FDA-reguleret enhedsprodukt
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .