CHS Nurses Clinical Competence in Detecting Signs of PPD in Non-Native Speaking Immigrant Mothers'

Sponsor
Lund University (Other)
Overall Status
Completed
CT.gov ID
NCT04167709
Collaborator
Region Skane (Other), Föreningen Mjölkdroppen Helsingborg (Other)
40
1
1
21.7
1.8

Study Details

Study Description

Brief Summary

The aim is to develop, test and evaluate an educational intervention with the purpose to strengthen Child Health Services (CHS) Nurses clinical competence in detecting signs of postpartum depression in non-native-speaking immigrant mothers. The pilot study has a pre-post experimental design. Data are collected before and after the intervention. The differences in the values of the collected data are used to estimate the effect of the intervention.

Condition or Disease Intervention/Treatment Phase
  • Other: Education in clinical competence in detecting signs of postpartum depression in immigrant mothers
N/A

Detailed Description

To be eligible for the study the CHS nurse must perform screening of immigrant mothers for postpartum depression with help of an interpreter according to the Edinburgh Postnatal Depression Scale (EPDS) method more than three times a year. The EPDS is a likert form scale with ten statements and is used in combination with a Clinical interview.

Approximately 40-45 CHS nurses will be enrolled in the pilot study. The number of nurses are calculated in comparison to two other published studies within the same context. The instruments Clinical Cultural Competence Training Questionnaire (CCCTQ) and General Self-Efficacy scale (GSE) will be used as primary outcomes measures. Data are collected before the first education day and after the second education day. Secondary outcomes are also collected in connection to the educational intervention and consists of reported yearly statistics; how many mothers were are offered screening, participated in screening, number of screenings preformed with help og an interpreter and number of mothers offered follow-up after participating in screening.

Study Design

Study Type:
Interventional
Actual Enrollment :
40 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Intervention Model Description:
The study has a pre-post experimental design.The study has a pre-post experimental design.
Masking:
None (Open Label)
Primary Purpose:
Health Services Research
Official Title:
Child Health Services Nurses Clinical Competence in Detecting Signs of Post Partum Depression in Non-Native-Speaking Immigrant Mothers' -Development, Testing and Evaluation of an Intervention
Actual Study Start Date :
Jun 9, 2019
Actual Primary Completion Date :
May 13, 2020
Actual Study Completion Date :
Mar 31, 2021

Arms and Interventions

Arm Intervention/Treatment
Experimental: Allocated CHS nurses

Primary and secondary baseline data are collected from the allocated CHS nurses before the study starts. The CHS nurses are then given the educational intervention and afterwards primary and secondary outcomes are collected again.

Other: Education in clinical competence in detecting signs of postpartum depression in immigrant mothers
Groupbased educational intervention aimed at nurses in the Child Health Services in strengthening clinical competence in detecting signs of postpartum depression in non-native-speaking immigrant mothers

Outcome Measures

Primary Outcome Measures

  1. Clinical Cultural Competence Training Questionnaire [the questionnaire are given before and directly after the educational intervention]

    measures change in the participants experienced cultural competence. Consist of 8 items. Responses are made on a 4-pointscale.The mean score is calculated by adding up the sum of all answers (range 8-32) and dividing it by 8. The higher score the better outcome.

  2. General Self Efficacy scale [the questionnaire are given before and directly after the educational intervention]

    measures change in the participants confidence in their own ability. Consist of 10 items. Responses are made on a 4-pointscale.The mean score is calculated by adding up the sum of all answers (range 10-40) and dividing it by 10. The higher score the better outcome.

Secondary Outcome Measures

  1. mothers offered to participate in screening [before the educational intervention are given and one year after the educational intervention are given]

    number of mothers offered to participate in screening for postpartum depression

  2. mothers participating in screening [before the educational intervention are given and one year after the educational intervention are given]

    number of mothers participating in screening for postpartum depression

  3. screening with help of interpreter [before the educational intervention are given and one year after the educational intervention are given]

    number of screenings performed with help of an interpreter

  4. mothers offered follow-up after screening [before the educational intervention are given and one year after the educational intervention are given]

    number of mothers offered follow-up after participating in screening for postpartum depression

Eligibility Criteria

Criteria

Ages Eligible for Study:
25 Years to 67 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Nurse specialized in Primary Healthcare Nursing or Pediatric Nursing

  • Employed in the Child Health Services in the County Scania in Sweden

  • Performing at minimum three screenings per year for postpartum depression, according to the EPDS-method, with help of an interpreter

Exclusion Criteria:

Contacts and Locations

Locations

Site City State Country Postal Code
1 Lund University Lund Scania Sweden 221 00

Sponsors and Collaborators

  • Lund University
  • Region Skane
  • Föreningen Mjölkdroppen Helsingborg

Investigators

  • Study Chair: Inger Kristensson Hallström, professor, Lund University, Faculty of Medicine, Department of Health Sciences

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Publications

Responsible Party:
Lund University
ClinicalTrials.gov Identifier:
NCT04167709
Other Study ID Numbers:
  • 2018/1063
First Posted:
Nov 19, 2019
Last Update Posted:
Sep 5, 2021
Last Verified:
Sep 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Lund University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 5, 2021