Feasibility of alcohol screening and brief intervention in primary health care in Kazakhstan - study protocol of a pilot cluster randomised trial

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Feasibility of alcohol screening and brief intervention in primary health care in Kazakhstan - study protocol of a pilot cluster randomised trial. / Schulte, Bernd; O'Donnell, Amy; Lahusen, Harald; Lindemann, Christina; Prilutskaya, Mariya; Yussopov, Oleg; Kaliyeva, Zhanar; Martens, Marcus-Sebastian; Verthein, Uwe.

In: PILOT FEASIBILITY ST, Vol. 6, 09.01.2020, p. 3.

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@article{9b0b29fe34f44991a1254b1fdaec5448,
title = "Feasibility of alcohol screening and brief intervention in primary health care in Kazakhstan - study protocol of a pilot cluster randomised trial",
abstract = "Background: Identifying and addressing heavy drinking represents a major public health priority worldwide. Whilst the majority of alcohol screening and brief intervention (ASBI) research has been conducted in western, high-income countries, evidence is growing that ASBI can also impact positively on heavy drinkers in low- and middle-income country populations. This mixed methods study aims to assess the feasibility of conducting a fully randomised controlled trial of the effectiveness of ASBI in primary care in Kazakhstan and explore the feasibility and acceptability of implementing ASBI in this setting from patients' and physicians' perspectives.Methods: Six primary health care units in the region of Pavlodar will be cluster randomised to either an intervention (WHO manualised 5 min alcohol brief intervention plus alcohol leaflet) or control group (simple feedback plus alcohol leaflet). Primary feasibility measures will be rates of participation at baseline and retention of eligible patients at the 3-month follow-up point. Patient/physician questionnaires and physician focus groups will assess additional dimensions of feasibility, as well as acceptability, according to the RE-AIM framework: Reach (rates of eligible patients screened/received advice); Effectiveness (change in AUDIT-C score); Adoption (rate/representativeness of participating physicians); Implementation (quality of ASBI/barriers and facilitators to delivery); and Maintenance (potential sustainability of intervention).Discussion: This is the first trial of the feasibility and acceptability of ASBI in Kazakhstan. As the planning and assessment of implementation determinants is based on the RE-AIM framework, the project outcomes will be relevant for the future development, tailoring and implementation of ASBI in Kazakhstan.Trial registration: DRKS, DRKS00015882, Registered 17 December 2018.",
author = "Bernd Schulte and Amy O'Donnell and Harald Lahusen and Christina Lindemann and Mariya Prilutskaya and Oleg Yussopov and Zhanar Kaliyeva and Marcus-Sebastian Martens and Uwe Verthein",
note = "{\textcopyright} The Author(s). 2020.",
year = "2020",
month = jan,
day = "9",
doi = "10.1186/s40814-019-0547-x",
language = "English",
volume = "6",
pages = "3",
journal = "PILOT FEASIBILITY ST",
issn = "2055-5784",
publisher = "BioMed Central Ltd.",

}

RIS

TY - JOUR

T1 - Feasibility of alcohol screening and brief intervention in primary health care in Kazakhstan - study protocol of a pilot cluster randomised trial

AU - Schulte, Bernd

AU - O'Donnell, Amy

AU - Lahusen, Harald

AU - Lindemann, Christina

AU - Prilutskaya, Mariya

AU - Yussopov, Oleg

AU - Kaliyeva, Zhanar

AU - Martens, Marcus-Sebastian

AU - Verthein, Uwe

N1 - © The Author(s). 2020.

PY - 2020/1/9

Y1 - 2020/1/9

N2 - Background: Identifying and addressing heavy drinking represents a major public health priority worldwide. Whilst the majority of alcohol screening and brief intervention (ASBI) research has been conducted in western, high-income countries, evidence is growing that ASBI can also impact positively on heavy drinkers in low- and middle-income country populations. This mixed methods study aims to assess the feasibility of conducting a fully randomised controlled trial of the effectiveness of ASBI in primary care in Kazakhstan and explore the feasibility and acceptability of implementing ASBI in this setting from patients' and physicians' perspectives.Methods: Six primary health care units in the region of Pavlodar will be cluster randomised to either an intervention (WHO manualised 5 min alcohol brief intervention plus alcohol leaflet) or control group (simple feedback plus alcohol leaflet). Primary feasibility measures will be rates of participation at baseline and retention of eligible patients at the 3-month follow-up point. Patient/physician questionnaires and physician focus groups will assess additional dimensions of feasibility, as well as acceptability, according to the RE-AIM framework: Reach (rates of eligible patients screened/received advice); Effectiveness (change in AUDIT-C score); Adoption (rate/representativeness of participating physicians); Implementation (quality of ASBI/barriers and facilitators to delivery); and Maintenance (potential sustainability of intervention).Discussion: This is the first trial of the feasibility and acceptability of ASBI in Kazakhstan. As the planning and assessment of implementation determinants is based on the RE-AIM framework, the project outcomes will be relevant for the future development, tailoring and implementation of ASBI in Kazakhstan.Trial registration: DRKS, DRKS00015882, Registered 17 December 2018.

AB - Background: Identifying and addressing heavy drinking represents a major public health priority worldwide. Whilst the majority of alcohol screening and brief intervention (ASBI) research has been conducted in western, high-income countries, evidence is growing that ASBI can also impact positively on heavy drinkers in low- and middle-income country populations. This mixed methods study aims to assess the feasibility of conducting a fully randomised controlled trial of the effectiveness of ASBI in primary care in Kazakhstan and explore the feasibility and acceptability of implementing ASBI in this setting from patients' and physicians' perspectives.Methods: Six primary health care units in the region of Pavlodar will be cluster randomised to either an intervention (WHO manualised 5 min alcohol brief intervention plus alcohol leaflet) or control group (simple feedback plus alcohol leaflet). Primary feasibility measures will be rates of participation at baseline and retention of eligible patients at the 3-month follow-up point. Patient/physician questionnaires and physician focus groups will assess additional dimensions of feasibility, as well as acceptability, according to the RE-AIM framework: Reach (rates of eligible patients screened/received advice); Effectiveness (change in AUDIT-C score); Adoption (rate/representativeness of participating physicians); Implementation (quality of ASBI/barriers and facilitators to delivery); and Maintenance (potential sustainability of intervention).Discussion: This is the first trial of the feasibility and acceptability of ASBI in Kazakhstan. As the planning and assessment of implementation determinants is based on the RE-AIM framework, the project outcomes will be relevant for the future development, tailoring and implementation of ASBI in Kazakhstan.Trial registration: DRKS, DRKS00015882, Registered 17 December 2018.

U2 - 10.1186/s40814-019-0547-x

DO - 10.1186/s40814-019-0547-x

M3 - SCORING: Journal article

C2 - 31938551

VL - 6

SP - 3

JO - PILOT FEASIBILITY ST

JF - PILOT FEASIBILITY ST

SN - 2055-5784

ER -