- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT02613624
Formative Research to Develop an Intervention Package to Promote Practice of Kangaroo Mother Care for Low Birth Weight and Preterm Infants in a Community (CKMC) (CKMC)
11. januar 2016 opdateret af: Society for Applied Studies
Formative Research to Develop an Intervention Package for Promotion of Kangaroo Mother Care for Low Birth Weight and Preterm Infants in a Community: In Preparation for a Randomized Controlled Trial to Examine Impact of Community Kangaroo Mother Care on Neonatal and Early Infant Mortality
The study is being conducted to develop an intervention to assess the feasibility of implementing Kangaroo Mother Care (KMC) for low birth weight (LBW) and preterm babies in a community setting.
A prototype intervention package will be developed using information obtained from in-depth interviews, focus group discussions and other qualitative research techniques.
These interviews will help us identify current behaviours, barriers to adoption of KMC and effective ways to promote KMC in the community.
The prototype intervention will be refined by conducting acceptability studies (household trials) with few mothers.
The study team are identifying LBW and preterm infants, demonstrating to mothers how to practice KMC and following up till KMC is stopped.
The process is being documented using observations and interviews.
Information is obtained on acceptability of KMC, number of hours per day and number of days KMC was given, breastfeeding practices and support provided by other family members.
Studieoversigt
Status
Afsluttet
Betingelser
Undersøgelsestype
Observationel
Tilmelding (Faktiske)
28
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
-
-
Haryana
-
Palwal, Haryana, Indien, 121102
- CHRD, Society for Applied Studies
-
-
Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
Ikke ældre end 1 uge (Barn)
Tager imod sunde frivillige
Ja
Køn, der er berettiget til at studere
Alle
Prøveudtagningsmetode
Ikke-sandsynlighedsprøve
Studiebefolkning
Rural and semi urban population of two primary health centre areas in two districts of the state of Haryana, India.
Beskrivelse
Inclusion Criteria:
- Low birth weight or preterm newborns
Exclusion Criteria:
- Babies with hospitalization criteria
- unable to feed or weight less than 1500 grams at birth
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Feasibility and acceptability of community based KMC
Tidsramme: 1 year
|
To determine whether community KMC is feasible to implement in the study setting and if so, can high enough adoption rates be achieved.
This will be ascertained by documenting proportion of mothers doing KMC, number of hours each day and number of days skin to skin contact is given.
|
1 year
|
|
Define intervention package
Tidsramme: 1 year
|
To define an intervention package, including the most effective way(s) to promote KMC in the study setting.
|
1 year
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Perceptions and practices of maternal and newborn care
Tidsramme: 1 year
|
To ascertain perceptions, beliefs and practices around pregnancy, delivery and maternal and newborn care.
Qualitative research methods such as focus group discussions, in-depth interviews and observations using open ended questionnaires, interview guides and checklists will be used.
|
1 year
|
|
Social norms around birthing practices
Tidsramme: 1 year
|
To identify social norms around birthing practices for normal, LBW infants and preterms.
Qualitative research methods such as focus group discussions, in-depth interviews and observations using open ended questionnaires, interview guides and checklists will be used.
|
1 year
|
|
Awareness and perception around KMC
Tidsramme: 1 year
|
To ascertain awareness and perceptions around KMC. Qualitative research methods such as focus group discussions, in-depth interviews and observations using open ended questionnaires, interview guides and checklists will be used.
|
1 year
|
|
Promotion of KMC
Tidsramme: 1 year
|
To identify ways to promote KMC in the community.
|
1 year
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Samarbejdspartnere
Efterforskere
- Ledende efterforsker: Sarmila Mazumder, MBBS, PhD, Centre for Health Research and Development, Society for Applied Studies, New Delhi
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart
1. april 2015
Primær færdiggørelse (Faktiske)
1. januar 2016
Studieafslutning (Faktiske)
1. januar 2016
Datoer for studieregistrering
Først indsendt
12. oktober 2015
Først indsendt, der opfyldte QC-kriterier
21. november 2015
Først opslået (Skøn)
24. november 2015
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Skøn)
12. januar 2016
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
11. januar 2016
Sidst verificeret
1. januar 2016
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- 2014/1913/REK vest
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 .
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