- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT04853693
Pregnancy Without Psychosocial Stress
Pregnancy Without Psychosocial Stress - the Earliest Prevention of Mental Disorders and Toxic Stress in Children
The project is aimed at children who are exposed to the toxic psychosocial stress present in their mothers during pregnancy or after childbirth. Due to psychosocial stress in their mothers, these children are at risk of developing a mental disorder or having impaired psychosocial development.
In Czechia, there is no prevention of psychosocial stress in women, which also plays a preventive role in the development of mental disorders in their children. Mental disorders in parents are stigmatized in Czechia, which prevents parents from seeking care.
The investigators want to change this situation, so they will:
- create and pilot a screening program for psychosocial stress in perinatal women in gynecological clinics
- connect the screening program to the integrated step care system created by the investigators, including peer support, which the investigators will test
Panoramica dello studio
Stato
Intervento / Trattamento
Descrizione dettagliata
ACTIVITY 1 Objective of the activity: To increase the support of mental health and well-being of unborn children and children in the period soon after their birth by early detection of women experiencing psychosocial stress during pregnancy and after childbirth. Target group: Pregnant women and postpartum women and their children.
Methods: Because the occurrence of symptoms of psychosocial stress in pregnancy is one of the main predictors of the development of mental disorders after childbirth, the investigators will test whether the introduction of screening in gynecological clinics during pregnancy reduces the incidence of untreated mental disorders in women 6 weeks after birth. Thanks to screening, the investigators want to capture women and their children who are exposed to toxic stress during pregnancy. Screening: Gynecological clinics will be equipped with a tablet with screening software (Czech version of the Edinburgh Perinatal Depression Scale; Perinatal Anxiety Screening Scale; Perinatal Psychosocial Profile). The software runs on the servers of the National Institute of Mental Health (NUDZ), secured against cybercrime. Work with data obtained during screening is subject to GDPR and the process is approved by the NUDZ Ethics Committee. The screening software is automated and sends the woman information about the results to her email.
Evaluation: a randomized controlled study in 20 gynecological clinics in 3 regions of the Czech Republic (Prague, Central Bohemia and Olomouc Region). Participating gynecological outpatient clinics will be randomized in a 1: 1 ratio into two groups: Intervention outpatient clinics: Intervention outpatient clinics offer study participation to all pregnant women during their pregnancy. Furthermore, all women checked at the end of the sixth week. Intervention clinics will also be equipped with information materials on mental health during pregnancy and after childbirth. Control clinics: actively offer participation to all women only at the control at the end of the sixth week postpartum. The main checkpoint in both groups of outpatient clinics is the 6th week after delivery, when the woman comes to the gynecological outpatient clinic for a mandatory check-up in Czechia. All women who will participate in Activity 1 will be examined by telephone using a structured psychiatric examination by a psychiatrist at the end of the 6th week after childbirth so that we can determine the presence of mental disorders.
Hypothesis: There are more women in control clinics who are not treated for a mental disorder at the end of the 6th week after delivery, even if they have been diagnosed, than in intervention clinics.
ACTIVITY 2 Objective of the activity: To increase the support of mental health and well-being of unborn children and children soon after their birth through early intervention in women experiencing psychosocial stress during pregnancy and after childbirth. Target group: Women who experience psychosocial stress during pregnancy and after childbirth and their children. Methods: Activity 2 is directly related to activity 1 of the submitted project. As part of Activity 2, the investigators will provide the women captured by the screening intervention developed by them.
Intervention: Mom supports Mom includes at least four telephone or other contacts - Skype, Zoom, WhatsApp, Facebook Messenger, ...) Between the project participant and a peer consultant trained by the National Institute of Mental Health and Mom´s Smile. Within peer support, the main methods are listening, psychoeducation, basic procedures of cognitive behavioral therapy and mindfulness, shared personal experiences with perinatal psychosocial stress and, if necessary, a reference to professional counseling (psychology, psychiatry).
Evaluation: a randomized controlled study in gynecological clinics participating in Activity 1 of the project. Women experiencing psychosocial stress, which we will screen through Activity 1, will be randomized 1: 1 into two groups: Intervention group: The peer consultant coordinator will connect the woman with the peer consultant who will carry out the intervention Mom supports mom. Control group: The woman will be sent automatic feedback with information on how to proceed if the participant wants to seek help herself. Evaluation of the effect of the intervention: The investigators evaluate depressive symptoms using the Edinburgh scale of perinatal depression; anxiety symptoms using the Perinatal Anxiety Screening Scale; psychosocial stress using the Perinatal Psychosocial Profile; quality of life using the 8-dimensional quality of life scale; and parental competences using the Parenting Sense of Competence Scale. The investigators collect data after the woman enters Activity 2 and one month after entering. The Investigators will evaluate the feedback from users using qualitative questions.
Hypothesis: Intervention Mom supports mom, reduces depressive and anxiety symptoms and general psychosocial stress in women experiencing psychosocial stress. Intervention Mom supports mom, increases the quality of life and parental competencies of women experiencing psychosocial stress.
Statistics: n = 120 (60 in each arm of the study). Sample size is calculated so that the investigators can detect a medium-to-large group difference in the scale of depressive symptoms (effect size = 0.6; t-test) at power 80%, significance level 5% (2-sided) and potential drop out 30 %.
Tipo di studio
Iscrizione (Anticipato)
Fase
- Non applicabile
Contatti e Sedi
Contatto studio
- Nome: Pavla Spadova, Ph.D.
- Numero di telefono: +420 283 088 111
- Email: Pavla.Spadova@nudz.cz
Luoghi di studio
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Klecany, Cechia, 25067
- Reclutamento
- National Institute of Mental Health
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Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
Accetta volontari sani
Sessi ammissibili allo studio
Descrizione
Inclusion Criteria ACTIVITY 1:
- sex-female
- pregnancy
- woman is registered during and after pregnancy in one of 20 study gynecological outpatient clinics
- signing informed consent
- email address ownership
- age 18-45
Inclusion Criteria ACTIVITY 2:
- Edinburgh Postpartum Depression Scale score ≥10.
- participant identified through the ACTIVITY 1 of the study
Exclusion Criteria ACTIVITY 1:
- acute medical illness or significant pregnancy complication (based on self-report)
Exclusion Criteria ACTIVITY 2:
- acute suicidal behavior (based on self-report)
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Prevenzione
- Assegnazione: Randomizzato
- Modello interventistico: Assegnazione parallela
- Mascheramento: Doppio
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
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Sperimentale: Mom´s Supporting Mom (MSM)
A preventive intervention that involves psychoeducation and peer techniques described in study detailed description.
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A preventive peer consultation intervention for Postpartum Depression.
Altri nomi:
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Comparatore attivo: Enhanced Treatment as Usual
Referral to treatment in the community and monitoring
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Referral to treatment in the community, clinical monitoring
Altri nomi:
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Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Postpartum depressive symptoms
Lasso di tempo: 6 weeks postpartum
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self-rated depressive symptomatology measured by Edinburgh Postnatal Depression Scale.
Score range 0-30, higher score represents worse outcome.
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6 weeks postpartum
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Treatment gap for postpartum mental disorders
Lasso di tempo: 6 weeks postpartum
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prevalence of untreated mental health disorders in postpartum women assessed by The Mini-International Neuropsychiatric Interview
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6 weeks postpartum
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Pregnancy depressive symptoms
Lasso di tempo: up to 32 weeks
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self-rated depressive symptomatology measured by Edinburgh Postnatal Depression Scale.
Score range 0-30, higher score represents worse outcome.
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up to 32 weeks
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Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Postpartum anxiety symptoms
Lasso di tempo: 6 weeks postpartum
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self-rated anxiety symptomatology measured by Perinatal Anxiety Screening Scale.
Score range 0-93, higher score represents worse outcome.
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6 weeks postpartum
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Pregnancy anxiety symptoms
Lasso di tempo: up to 32 weeks
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self-rated anxiety symptomatology measured by Perinatal Anxiety Screening Scale.
Score range 0-93, higher score represents worse outcome.
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up to 32 weeks
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Altre misure di risultato
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Psychosocial stress factors
Lasso di tempo: through study completion, an average of 1 year
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self-rated psychosocial stress factors measured by Prenatal psychosocial profile.
Score range 11 - 44, higher score represents worse outcome.
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through study completion, an average of 1 year
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Prenatal mother-baby attachment
Lasso di tempo: up to 32 weeks
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self-report measure of maternal-fetal attachment measured by Prenatal Attachment Inventory
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up to 32 weeks
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Parenting competences
Lasso di tempo: 6 weeks postpartum
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self-report measure od maternal sense of parenting competence measured by Parenting Sense of Competence Scale
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6 weeks postpartum
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Collaboratori e investigatori
Investigatori
- Investigatore principale: Antonin Sebela, Ph.D., National Institute of Mental Health, Klecany, Czechia
Studiare le date dei record
Studia le date principali
Inizio studio (Effettivo)
Completamento primario (Anticipato)
Completamento dello studio (Anticipato)
Date di iscrizione allo studio
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Effettivo)
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Termini MeSH pertinenti aggiuntivi
Altri numeri di identificazione dello studio
- ZD-ZDOVA1-018
Piano per i dati dei singoli partecipanti (IPD)
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Descrizione del piano IPD
Periodo di condivisione IPD
Criteri di accesso alla condivisione IPD
Tipo di informazioni di supporto alla condivisione IPD
- Modulo di consenso informato (ICF)
Informazioni su farmaci e dispositivi, documenti di studio
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Prove cliniche su Depressione, dopo il parto
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Halic UniversityNon ancora reclutamentoDolore lombopelvico postpartum | Mal di schiena postpartum | Dolore della Cintura Pelvica PostpartumTurchia (Türkiye)
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Northwestern UniversityReclutamento
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The University of Texas Health Science Center,...CompletatoPostpartum | Turni di mediciStati Uniti
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Assistance Publique Hopitaux De MarseilleSconosciuto
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Selcuk UniversitySelcuk University Scientific Research Projects UnitReclutamento
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Cairo UniversityReclutamento
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FHI 360Ghana Health Services; Ministry of Health, ZambiaCompletatoPeriodo postpartumGhana, Zambia
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London School of Hygiene and Tropical MedicineDepartment for International Development, United Kingdom; Economic and Social... e altri collaboratoriCompletatoPeriodo postpartumBurkina Faso
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University of North Carolina, Chapel HillSociety of Family PlanningCompletatoContraccezione postpartumStati Uniti
Prove cliniche su Mom´s Supporting Mom
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Inova Health Care ServicesUniversity of Houston; University of Louisville; Howard University; Tigerlily Foundation e altri collaboratoriCompletatoMelanoma | Cancro | Cancro al seno | Cancro testa e collo | Cancro ginecologico | Cancro colorettale | Cancro esofageo | Cancro ai polmoni | Cancro al cervello | Cancro gastrointestinale | Cancro del sistema nervoso centrale | Terapia dell'accettazione e dell'impegno | Cancro del sangue | Cancro genito-urinario | Intervento... e altre condizioniStati Uniti
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Children's Hospital of PhiladelphiaWilliam Penn FoundationCompletato
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Institut de Recherche pour le DeveloppementMedical Research Council; Institut Pasteur; Centre Muraz; REVS PLUS Burkina Faso; Young... e altri collaboratoriReclutamentoHIV | HBV | SifilideBurkina Faso, Gambia
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Perelel Inc.University of GeorgiaReclutamento
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San Diego State UniversityEl Colegio de la Frontera NorteReclutamento
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University of MichiganCompletatoGravidanza | Periodo postpartum
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Anabio R&DHanoi Obstetrics and Gynecology HospitalNon ancora reclutamentoPerdita di peso | Disturbi funzionali gastrointestinali (FGID)Vietnam
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Rush University Medical CenterNational Institute on Minority Health and Health Disparities (NIMHD); Ohio State...CompletatoNascita prematura | Neonato, peso alla nascita molto basso | Latte, umano | Pompaggio, SenoStati Uniti
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Tulane UniversityNational Institute of Mental Health (NIMH)CompletatoPsicopatologiaStati Uniti
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University of Wisconsin, MadisonCompletatoIncontinenza, urinaria | Incontinenza intestinaleStati Uniti