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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02628184
Other study ID # 13383
Secondary ID 170005
Status Completed
Phase
First received
Last updated
Start date January 2016
Est. completion date September 2016

Study information

Verified date June 2021
Source University of Southampton
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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.


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.


Recruitment information / eligibility

Status Completed
Enrollment 19
Est. completion date September 2016
Est. primary completion date September 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility 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 Design


Related Conditions & MeSH terms


Intervention

Other:
Maternity Services Development Programme
The Maternity Services Development Programme was implemented to improve care for local families (service users) involved with maternity services. The aim was to improve care during the early stages of a family's development and to establish foundations for long-term well-being. One aspect of the programme worked to improve the delivery of care by facilitating collaboration and joint-planning between service providers. The programme uses local city Children's Centres to co-locate services (different agencies or professionals who are working within the same locality). The aim of co-location was to promote stronger collaboration between maternity services and other service provider agencies to develop stronger partnerships, and to help identify those who are (or who may become) vulnerable.

Locations

Country Name City State
United Kingdom Buckland Children's Centre Portsmouth Hampshire
United Kingdom Mitlon Park Children's Centre Portsmouth Hampshire
United Kingdom Paulsgrove Children's Centre Portsmouth Hampshire
United Kingdom Somerstown Children's Centre Portsmouth Hampshire

Sponsors (1)

Lead Sponsor Collaborator
University of Southampton

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Perceived benefits or challenges of collaborative working 2 Years
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