A Case Study of a Maternity Service Development Programme

June 11, 2021 updated by: University of Southampton

A Case Study of a Maternity Service Development Programme and Its Influence on Inter-agency Collaboration

BACKGROUND: In 2011 a Maternity Services Development Programme was implemented in a South of England city, to promote effective collaborative working between maternity services (midwives) and other service providers (health visitors, social workers, specialist services etc.) by co-locating services in local childrens centres. The progamme ultimately aimed to improve care for local service users (women and their families), especially those considered vulnerable. Implemented changes were based on evidence that suggests poor collaborative working contributes to poorer outcomes. RATIONALE: To explore the impact of the programme on local service providers, and by association service user care. AIM: To explore a localised Maternity Services Development Programme, identifying how inter- agency collaborative working occurs, and the service providers perceived benefits and challenges on collaboration, and by association service user care. METHODOLOGY: The proposed research uses a case study approach to collect and analyse predominantly qualitative data, and some quantitative data. Data will be collected using observation episodes (e.g. participant meetings) to observe collaboration, and interviews to explore these experiences. Additionally documents will be analysed to observe documented evidence of collaborative practice. Pre-existing statistical data will also be used to highlight changes in indicators of service user well being since the implementation of the Maternity Services Development Programme. PARTICIPANTS: A cross-section of service providers (no service users) working in or with maternity services from 4 of 9 city Children Centre's. FINDINGS: No current findings, data collection expected to start September 2015.

Study Overview

Status

Completed

Conditions

Detailed Description

In 2011 a Maternity Services Development Programme (MSDP) was implemented in one South of England city. The programme aimed to promote effective collaborative working between maternity services (midwives) and other service providers (health visitors, social workers, Children Centre staff, specialist and volunteer services) to improve outcomes for service users (women and families). The MSDP utilised local Children's Centres, which provide community focused family support, to co-locate maternity services and other service providers. The rationale to improve collaborative working is supported by evidence suggesting poor collaborative working contributes to poorer outcomes (Laming Report 2003; Marmot Review 2010). Therefore programmes such as the MSDP could potentially improve short and long-term outcomes for those accessing maternity services.

The proposed research uses a case study approach to collect and analyse predominantly qualitative data, and some quantitative data. This method will allow for analysis of the MSDP and understanding of its influence on maternity services and collaboration, and will aim to illuminate perceived strengths and challenges of the MSDP evident to services providers. Data will be collected using observation episodes (e.g. participant meetings) to observe collaboration, and interviews to explore experiences. Additionally documents will be analysed to observe documented evidence of collaborative practice. Pre-existing statistical data will also be used to highlight changes in indicators of service user well-being since the implementation of the MSDP.

The research will recruit a cross-section of service providers (no service users) that work in or with maternity services from four of the nine city Children Centres. Invitation letters will be circulated to potential participants through participating Children Centre management, where they will be invited to participate in the observation and interview data collection activities. They will then be able to select the extent of their participation.

Study Type

Observational

Enrollment (Actual)

19

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Hampshire
      • Portsmouth, Hampshire, United Kingdom, PO1 4PN
        • Buckland Children's Centre
      • Portsmouth, Hampshire, United Kingdom, PO4 8EU
        • Mitlon Park Children's Centre
      • Portsmouth, Hampshire, United Kingdom, PO5 4LP
        • Somerstown Children's Centre
      • Portsmouth, Hampshire, United Kingdom, PO6 3LP
        • Paulsgrove Children's Centre

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

Service provider practitioners that have been influenced by the implementation of the Maternity Services Development Programme (including, Children Centre Staff and Practitioners (Centre Lead Practitioner/Manager, Family and Child practitioner and Frontline Receptionist), Midwives, Health Visitors, Social Workers and Additional Professional Practitioners (Nurture Practitioner, Parenting Practitioner and Early Years Teacher). Volunteer agencies have been excluded as many local groups are made up from community service users.

Description

The inclusion criteria for this study is:

  • Service providers working in, or from a local city Children's Centre (this may be in a practice base or working in the community);
  • Service providers working in, or with maternity services;
  • Service providers caring for families with women who are pregnant, or under the remit of maternity services (typically up to and including 6 weeks post-natally).

The exclusion criteria for this study is:

  • Service providers caring for families with women no longer under the remit of maternity services (typically over 6 weeks post-natally).
  • Service users (all women and families who use maternity services, inclusive of those considered vulnerable - this may be inclusive of some volunteer organisations who also provide services within children's centres).

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Perceived benefits or challenges of collaborative working
Time Frame: 2 Years
2 Years

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Director: Elizabeth Cluett, University of Southampton
  • Study Director: Jane March-McDonald, University of Southampton

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

January 1, 2016

Primary Completion (Actual)

September 1, 2016

Study Completion (Actual)

September 1, 2016

Study Registration Dates

First Submitted

July 14, 2015

First Submitted That Met QC Criteria

December 8, 2015

First Posted (Estimate)

December 11, 2015

Study Record Updates

Last Update Posted (Actual)

June 16, 2021

Last Update Submitted That Met QC Criteria

June 11, 2021

Last Verified

June 1, 2021

More Information

Terms related to this study

Other Study ID Numbers

  • 13383
  • 170005 (Other Identifier: NHS)

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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