- ICH GCP
- Rejestr badań klinicznych w USA
- Badanie kliniczne NCT04279093
Digital Assessment of Well-being in New Parents (DAWN-P)
Digital Assessment of Well-being in New Parents (DAWN-P)
The mental health of new parents around the time of the birth of their baby has been identified as a key priority in the NHS (National Health Service) Long Term plan. At present, there is no nationally implemented method for monitoring parents' mental health, although the use of the Edinburgh Postnatal Depression Scale (EPDS) has been recommended. This is a paper based questionnaire administered by health visitors in the postnatal period. For the purposes of this project, the investigators contacted health visitors in Manchester to find out how they use EPDS in practice. Currently, health visitors only use the questionnaire if they feel there is a need during visits, and the questionnaire is not kept (only the overall score). Since almost 20% of mums develop postnatal depression, more systematic and thorough screening is needed.
The investigators developed an app version of the EPDS which takes less than 2 minutes to complete on a smartphone. It is anticpated that this will be a more accessible and practical method of conducting this important assessment. This project is a feasibility study to find out whether an app would be a feasible, acceptable, valid and safe way to monitor perinatal mental health in women and their partners.
The investigators aim to recruit 20 women and their partners in late pregnancy (after 36 weeks gestation) and ask them to use the app. The app will prompt completion of the EPDS once per day until 6 weeks postnatally. Participants' responses on the app will be transferred to a secure server at the University of Manchester. Participants will be invited to complete a paper version of the EPDS at the beginning and end of the study to check validity. They will also be asked to complete a questionnaire measuring the acceptability of the app and to take part in a brief qualitative interview at the end of the study.
Przegląd badań
Status
Warunki
Interwencja / Leczenie
Typ studiów
Zapisy (Rzeczywisty)
Kontakty i lokalizacje
Lokalizacje studiów
-
-
Greater Manchester
-
Manchester, Greater Manchester, Zjednoczone Królestwo, M13 9PL
- University of Manchester
-
-
Kryteria uczestnictwa
Kryteria kwalifikacji
Wiek uprawniający do nauki
Akceptuje zdrowych ochotników
Płeć kwalifikująca się do nauki
Metoda próbkowania
Badana populacja
Opis
The investigators aim to recruit 20 women in late pregnancy from the Antenatal Assessment Unit and the Antenatal Clinic at St Mary's Hospital, Manchester. Their partners will be invited to participate where applicable.
Inclusion criteria for pregnant women:
- after 36 weeks gestation
- aged over 18 years
- fluent in English
- under the care of Manchester University NHS Foundation Trust
Exclusion criteria for pregnant women:
- current stillbirth (women experiencing a stillbirth during the study will be withdrawn from the study)
- fetal abnormality
- multiple pregnancy
Inclusion criteria for partners:
- male or female partners of a mum participating in the study
- aged over 18
- fluent in English.
Plan studiów
Jak projektuje się badanie?
Szczegóły projektu
- Modele obserwacyjne: Kohorta
- Perspektywy czasowe: Spodziewany
Kohorty i interwencje
Grupa / Kohorta |
Interwencja / Leczenie |
---|---|
Pregnant/postpartum women and their partners
The investigators aim to recruit 20 women in late pregnancy from the Antenatal Assessment Unit and the Antenatal Clinic at St Mary's Hospital. Their partners will be invited to participate where applicable. Inclusion and exclusion criteria for pregnant women are as follows:
Inclusion criteria for partners: male or female partners of a mum participating in the study, aged over 18 and fluent in English. |
No intervention, but participants will use a smartphone app daily (ClinTouch DAWN-P) to complete the Edinburgh Postnatal Depression Scale
|
Co mierzy badanie?
Podstawowe miary wyniku
Miara wyniku |
Opis środka |
Ramy czasowe |
---|---|---|
Percentage of app based EPDS (Edinburgh Postnatal Depression Scale) assessments completed during the app-use phase
Ramy czasowe: 36 weeks gestation until 6 weeks postpartum
|
Percentage of app based EPDS (Edinburgh Postnatal Depression Scale) assessments completed during the app-use phase
|
36 weeks gestation until 6 weeks postpartum
|
Percentage of eligible individuals recruited to the study
Ramy czasowe: Baseline
|
Percentage of eligible individuals recruited to the study
|
Baseline
|
Dropout rate - percentage of participants who consent to take part in the study dropping out during the app use phase
Ramy czasowe: 36 weeks gestation until 6 weeks postpartum
|
Percentage of participants who consent to take part in the study dropping out during the app use phase
|
36 weeks gestation until 6 weeks postpartum
|
Percentage of participants completing at least a third of app-based assessments
Ramy czasowe: 36 weeks gestation until 6 weeks postpartum
|
Percentage of participants completing at least a third of app-based assessments.
The a priori "accept" criterion will be >33% data points completed
|
36 weeks gestation until 6 weeks postpartum
|
Percentage of participants completing at least half of app-based assessments
Ramy czasowe: 36 weeks gestation until 6 weeks postpartum
|
Percentage of participants completing at least half of app-based assessments.
The a priori target criterion will be 50% of participants submitting at least 50% of app-based assessments.
|
36 weeks gestation until 6 weeks postpartum
|
Miary wyników drugorzędnych
Miara wyniku |
Opis środka |
Ramy czasowe |
---|---|---|
Transcripts from qualitative interviews with parents who have used the screening app regarding acceptability of the app
Ramy czasowe: 6 weeks postpartum
|
Transcripts from qualitative interviews with parents who have used the screening app regarding acceptability of the app
|
6 weeks postpartum
|
abridged Mobile App Rating Scale
Ramy czasowe: 6 weeks postpartum
|
abridged Mobile App Rating Scale score
|
6 weeks postpartum
|
Edinburgh Postnatal Depression Scale - app-based version
Ramy czasowe: 36 weeks gestation until 6 weeks postpartum
|
Edinburgh Postnatal Depression Scale - app-based version
|
36 weeks gestation until 6 weeks postpartum
|
Edinburgh Postnatal Depression Scale - paper version
Ramy czasowe: 36-37 weeks gestation; 5-6 weeks postpartum
|
Edinburgh Postnatal Depression Scale - paper version
|
36-37 weeks gestation; 5-6 weeks postpartum
|
Number of adverse events occurring during the app-use phase of the study
Ramy czasowe: 36 weeks gestation until 6 weeks postpartum
|
Number of adverse events occurring during the app-use phase of the study
|
36 weeks gestation until 6 weeks postpartum
|
Qualitative interview data on participants' experience of using the app.
Ramy czasowe: 6 weeks postpartum
|
Qualitative interview data on participants' experience of using the app.
|
6 weeks postpartum
|
Demographic questionnaire
Ramy czasowe: Baseline (36 weeks pregnant)
|
Demographic questionnaire asking standard questions about participants' demographic characteristics - e.g.
age, gender, employment status.
|
Baseline (36 weeks pregnant)
|
BMI (from casenotes)
Ramy czasowe: Baseline (36 weeks pregnant)
|
BMI (from casenotes)
|
Baseline (36 weeks pregnant)
|
past psychiatric history as reported in casenotes (any history of major depression, previously prescribed psychiatric medication, previously referred for talking therapy)
Ramy czasowe: Baseline (36 weeks pregnant)
|
past psychiatric history as reported in casenotes (any history of major depression, previously prescribed psychiatric medication, previously referred for talking therapy)
|
Baseline (36 weeks pregnant)
|
Answers to mental health screening questions at booking appointment (NICE, 2014: section 1.5.4)
Ramy czasowe: Baseline (36 weeks pregnant)
|
Answers to mental health screening questions at booking appointment (NICE, 2014: section 1.5.4)
|
Baseline (36 weeks pregnant)
|
Details of current childbirth (mode of delivery, live/still birth, any major obstetric complications)
Ramy czasowe: Baseline (36 weeks pregnant)
|
Details of current childbirth (mode of delivery, live/still birth, any major obstetric complications)
|
Baseline (36 weeks pregnant)
|
parity (total number of pregnancies reaching viable gestational age)
Ramy czasowe: Baseline (36 weeks pregnant)
|
parity (total number of pregnancies reaching viable gestational age)
|
Baseline (36 weeks pregnant)
|
Współpracownicy i badacze
Sponsor
Współpracownicy
Publikacje i pomocne linki
Daty zapisu na studia
Główne daty studiów
Rozpoczęcie studiów (Rzeczywisty)
Zakończenie podstawowe (Rzeczywisty)
Ukończenie studiów (Rzeczywisty)
Daty rejestracji na studia
Pierwszy przesłany
Pierwszy przesłany, który spełnia kryteria kontroli jakości
Pierwszy wysłany (Rzeczywisty)
Aktualizacje rekordów badań
Ostatnia wysłana aktualizacja (Rzeczywisty)
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
Ostatnia weryfikacja
Więcej informacji
Terminy związane z tym badaniem
Słowa kluczowe
Dodatkowe istotne warunki MeSH
Inne numery identyfikacyjne badania
- 274007
Plan dla danych uczestnika indywidualnego (IPD)
Planujesz udostępniać dane poszczególnych uczestników (IPD)?
Opis planu IPD
Informacje o lekach i urządzeniach, dokumenty badawcze
Bada produkt leczniczy regulowany przez amerykańską FDA
Bada produkt urządzenia regulowany przez amerykańską FDA
Te informacje zostały pobrane bezpośrednio ze strony internetowej clinicaltrials.gov bez żadnych zmian. Jeśli chcesz zmienić, usunąć lub zaktualizować dane swojego badania, skontaktuj się z register@clinicaltrials.gov. Gdy tylko zmiana zostanie wprowadzona na stronie clinicaltrials.gov, zostanie ona automatycznie zaktualizowana również na naszej stronie internetowej .