Region Örebro County
Örebro, 70185, Sweden
NCT Number: NCT04799860
The study will support implementation of a health promotive work-way in primary care setting by using external and internal facilitators, with the aim to identify effective implementation strategies and to evaluate intervention uptake. Data will be collected from multiple perspecitves.
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Notify Me18 year and older
All sexes
Interventional
Not applicable
Örebro, 70185, Sweden
Insufficient physical activity, hazardous use of alcohol, tobacco use and unhealthy eating habits increase the risk of cardiovascular diseases, cancer and type 2-diabetes. Health-promoting work reduces the disease risk and mortality and should thus be integrated in clinical care processes.
Despite support by the National guideline for prevention and treatment of unhealthy life-style habits, there is a chasm to bridge when integrating evidence into clinical practise. Prerequisites for changing work-ways are often underestimated and left to the individual co-workers to full fill on their own.
Too few patients are asked about life-style habits and too few receive evidence-based measures. The measures taken may also depend on sex, language, residence and caregiver's profession. The investigators strive to support the implementation of a health-promoting way of working that includes self-reporting of life-style habits before a visit and that takes measures for those with at least one unhealthy lifestyle habit.
The aim is to identify effective implementation strategies for health-promoting efforts in the primary care. The perceptions of barriers and opportunities when changing way of working from the target groups (leaders, co-workers, patients) will be used to enhance the possibility of successful implementation. Strategies are enhanced by theories of leading change. External and internal facilitators support the implementation.
The study will evaluate the effects and the implementation process at the level of leaders, patients, co-workers, facilitators and organisation in short (4-6 months) and long term (16-18 months).
The project provides generalizable knowledge on strategies to overcome the gap between evidence and praxis, contributing to utilize an existing synthesized knowledgebase regarding health-promoting and preventative workways in a Swedish primary care setting.
It is central for the health care system to identify successful implementation strategies in order to manage their future mission.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
for co-workers:
Inclusion criteria
for patients filling in the study specific questionnaire:
Inclusion criteria
for personcentered processmapping:
Inclusion criterina for managers:
Clinical intervention: The patient is asked to fill in a screening form with life-style related questions. The caregiver takes adequate measures according to the recommendations of the national guideline and the filled in screeing form. The caregiver documents the measures taken.
Implementation intervention as described previously: using tailored strategies to support implementation of the gudieline-based recommendations
Time frame: Change from baseline (6 months), through study completion up to 6 months after end of implementation support
specific codes are used for measures related to the guideline recommendations for grade of advice for insufficient physical activity, unhealthy eating habits, hazardous use of alcohol and tobacco use and prescribed physical activity
Time frame: Change from baseline (6 months), through study completion up to 18 months after end of implementation support
specific codes are used for measures related to the guideline recommendations for grade of advice for insufficient physical activity, unhealthy eating habits, hazardous use of alcohol and tobacco use and prescribed physical activity
Time frame: Change from baseline S-Nomad score up to 4 to 6 months after end of study completion
23-item questionnaire covering the constructs coherence, cognitive participation, collective action and reflexive monitoring
Time frame: Change from baseline S-Nomad score up to 16 to 18 months after end of study completion
23-item questionnaire covering the constructs coherence, cognitive participation, collective action and reflexive monitoring
Time frame: Change from baseline up to 4 to 6 months after end of implementation support
Questions related to the patients' perception on receiving the clinical intervention or not
Time frame: Change from baseline in AIM,IAM and FIM up to 4 to 6 months after end of implementation support
Appropriateness, feasability, acceptability of the clinical intervention is rated on a 5-graded scale with 4 items per construct
Time frame: Change from baseline in AIM,IAM and FIM up to 16 to18 months after end of implementation support
Appropriateness, feasability, acceptability of the clinical intervention is rated on a 5-graded scale with 4 items per construct
Time frame: Interviews pre-intervention and up to 3 to 6 months after end of implementation support
Semi-structured interview guides directed to facilitators, co-workers and managers
Time frame: Interviews pre-intervention and up to 16 to18 months after end of implementation support
Semi-structured interview guides directed to facilitators, co-workers and managers
Time frame: At baseline
Structured workshop with patient representatives
Time frame: Through study completion, in average 16 months
To measure fidelity, dose and reach and changes at the unit that may affect the implementation process
Region Örebro County
Other
Act in Time- Implementation of Health Promotive Work-way in Primary Care Setting - Evaluation of Effect- and Implementation Process (AcTi)
Acronym: AcTi
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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