Summary information

Study title

Participation and Representation in Health Policy : The Role of Health Consumer Groups, 1999

Creator

Allsop, J., De Montfort University, Department of Public Policy
Baggott, R., De Montfort University, Department of Public Policy
Jones, K., De Montfort University, Department of Public Policy

Study number / PID

4461 (UKDA)

10.5255/UKDA-SN-4461-1 (DOI)

Data access

Restricted

Series

Not available

Abstract

Abstract copyright UK Data Service and data collection copyright owner.


The aims of this study were:
to explore how a sample of national health consumer groups represents the interests of patients, users and carers within the policy process through analysing their aims, objectives and strategies; examining their internal organisation and relationship with their members and grass-roots support; investigating how professional and business interests are incorporated and financial resources are mobilised.
to describe and analyse how these health consumer groups interact with central government departments and agencies, Parliament, and the media in relation to policy making.
to examine alliances between specific health consumer groups and investigate the particular role of umbrella consumer organisations in promoting alliances.
to assess the contribution of theoretical perspectives and models to an understanding of the role of health consumer groups and in particular to assess whether different strategies and modes of interaction are related to group characteristics.
Main Topics:

The dataset contains information relating to the internal structure and activities of health consumer groups in five disease condition areas (arthritis, cancer, heart and circulatory disease, maternity and childbirth and mental health). Groups with an interest in more than one of these condition areas are also included. Data are provided on their date of formation, income, membership and decision-making body. Contact with government and other stakeholders is logged, as are their views on facilitators and barriers to the policy process.

Methodology

Data collection period

01/01/1999

Country

United Kingdom

Time dimension

Cross-sectional (one-time) study

Analysis unit

Groups
National
Health consumer groups

Universe

Health consumer groups in the arthritis, cancer, heart and circulatory disease, maternity and childbirth and mental health sectors (including those whose interests span more than one of the categories), in the UK during 1999.

Sampling procedure

groups in the disease condition sectors specified.

Kind of data

Numeric

Data collection mode

Postal survey

Funding information

Grant number

R000237888

Access

Publisher

UK Data Service

Publication year

2002

Terms of data access

The Data Collection is available to UK Data Service registered users subject to the End User Licence Agreement.

Commercial use of the data requires approval from the data owner or their nominee. The UK Data Service will contact you.

Related publications

  • Allsop, J., Jones, K. and Baggott, R. (2004) 'Pain, loss and collective action:: health consumer groups and the policy process' in I. Shaw and K. Kauppinen (eds.), , Aldershot: Ashgate Publishing. ISBN075-4632768 | 978-0754632764
  • Allsop, J., Baggott, R. and Jones, K. (2004) 'Influencing the National Policy Process:: the Role of Health Consumer Groups', Health Expectations, 18-28
  • Baggott, R., Allsop, J. and Jones, K. (2002) 'Health consumers and the national policy process' in S. Henderson and A. Petersen (eds.), , London: Routledge, 48-65. ISBN041-5259495 | 978-0415259484
  • Baggott, R., Jones, K. and Allsop, J. (2000) 'Under the influence', Health Service Journal, 28-29