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    Conflict and user involvement in drug misuse treatment decision-making: a qualitative study.

    Source

    School of Environment and Development, The University of Manchester, Oxford Road, Manchester, M13 9PL, UK. jan.fischer@postgrad.manchester.ac.uk

    Abstract

    BACKGROUND:

    This paper examines client/staff conflict and user involvement in drug misuse treatment decision-making.

    METHODS:

    Seventy-nine in-depth interviews were conducted with new treatment clients in two residential and two community drug treatment agencies. Fifty-nine of these clients were interviewed again after twelve weeks. Twenty-seven interviews were also conducted with staff, who were the keyworkers for the interviewed clients.

    RESULTS:

    Drug users did not expect, desire or prepare for conflict at treatment entry. They reported few actual conflicts within the treatment setting, but routinely discussed latent conflicts--that is, negative experiences and problematic aspects of current or previous treatment that could potentially escalate into overt disputes. Conflict resulted in a number of possible outcomes, including the premature termination of treatment; staff deciding on the appropriate outcome; the client appealing to the governance structure of the agency; brokered compromise; and staff skilfully eliciting client consent for staff decisions.

    CONCLUSION:

    Although the implementation of user involvement in drug treatment decision-making has the potential to trigger high levels of staff-client conflict, latent conflict is more common than overt conflict and not all conflict is negative. Drug users generally want to be co-operative at treatment entry and often adopt non-confrontational forms of covert resistance to decisions about which they disagree. Staff sometimes deploy user involvement as a strategy for managing conflict and soliciting client compliance to treatment protocols. Suggestions for minimising and avoiding harmful conflict in treatment settings are given.

    PMID:
    18837989
    [PubMed - indexed for MEDLINE]
    PMCID:
    PMC2569024
    Free PMC Article

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