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出境医 / 临床实验 / CUlturally Sensitive TOols for Ethnic Minorities in Diabetes Self-management Education and Support (CUSTOM)

CUlturally Sensitive TOols for Ethnic Minorities in Diabetes Self-management Education and Support (CUSTOM)

Study Description
Brief Summary:
The CUSTOM research project represents a complex intervention. The project aim of the intervention is, through the delivery of culturally sensitive Diabetes self-management education and support, to support ethnic minorities with type 2 diabetes in making health-promoting decisions about their care and gaining insight into their goals, values and motivation to improve their daily diabetes self-management. The target group comprises ethnic minorities whose native language is Arabic, Urdu or Turkish.

Condition or disease Intervention/treatment
Diabetes Mellitus, Type 2 Other: Group course

Show Show detailed description
Study Design
Layout table for study information
Study Type : Observational
Estimated Enrollment : 309 participants
Official Title: CUlturally Sensitive TOols and Methods for Ethnic Minorities (CUSTOM): Building Bridges Between Theory and Practice in Diabetes Self-management Education and Support
Actual Study Start Date : March 1, 2019
Estimated Primary Completion Date : December 31, 2020
Estimated Study Completion Date : October 2022
Arms and Interventions
Group/Cohort Intervention/treatment
Intervention, Centre for Diabetes or local setting
Group-based course in diabetes education including 6 sessions of approximately 3 hours. Sessions are constructed around themes such as; diabetes knowledge and complication, mental health, diet, physical activity, Ramadan, medicine and include practical exercises such as blood sugar measurements, walking etc.
Usual care
Usual care in 5 municipalities in the west area of Copenhagen
Other: Group course
Education and support

Outcome Measures
Primary Outcome Measures :
  1. Well-being [ Time Frame: 6 months ]
    questionnaire

  2. diabetes self-management [ Time Frame: 6 months ]
    questionnaire

  3. HbA1c [ Time Frame: 6 months ]
    blood sample


Eligibility Criteria
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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population
Referred to rehabilitation by the GP and has type 2 diabetes
Criteria

Inclusion Criteria:

  • Clinical diagnosis of type 2 diabetes
  • Ability to give written consent
  • Ability and willingness to attend and participate in a group-based education programme.
  • First language is Arabic, Turkish or Urdu.

Exclusion Criteria:

  • Physical illness that could seriously reduce their life expectancy and ability to participate in the trial
  • Mental illness that could reduce their ability to participate in the trial
  • Significant alcohol or substance misuse which could limit the participants ability to participate in the trial
  • A primary diagnosis of learning disability
  • Pregnancy, breastfeeding or plans of pregnancy during the study period
Contacts and Locations

Contacts
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Contact: Nana F Hempler, PhD +45 40732591 nana.folmann.hempler@regionh.dk
Contact: Lone B Rasmussen, PhD +45 22857377 lone.banke.rasmussen@regionh.dk

Locations
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Denmark
Centre for Diabetes Recruiting
Copenhagen, Denmark, 1620
Contact: Charlotte Glümer, MD, PhD       FS0H@kk.dk   
Contact: Gritt-Marie H Malling    +45 2910 6797    QI4M@kk.dk   
Sponsors and Collaborators
Steno Diabetes Center Copenhagen
Center for Diabetes, Copenhagen Municipality
Investigators
Layout table for investigator information
Principal Investigator: Nana F Hempler, PhD Steno Diabetes Center Copenhagen
Tracking Information
First Submitted Date May 13, 2019
First Posted Date May 15, 2019
Last Update Posted Date October 22, 2020
Actual Study Start Date March 1, 2019
Estimated Primary Completion Date December 31, 2020   (Final data collection date for primary outcome measure)
Current Primary Outcome Measures
 (submitted: May 13, 2019)
  • Well-being [ Time Frame: 6 months ]
    questionnaire
  • diabetes self-management [ Time Frame: 6 months ]
    questionnaire
  • HbA1c [ Time Frame: 6 months ]
    blood sample
Original Primary Outcome Measures Same as current
Change History
Current Secondary Outcome Measures Not Provided
Original Secondary Outcome Measures Not Provided
Current Other Pre-specified Outcome Measures Not Provided
Original Other Pre-specified Outcome Measures Not Provided
 
Descriptive Information
Brief Title CUlturally Sensitive TOols for Ethnic Minorities in Diabetes Self-management Education and Support
Official Title CUlturally Sensitive TOols and Methods for Ethnic Minorities (CUSTOM): Building Bridges Between Theory and Practice in Diabetes Self-management Education and Support
Brief Summary The CUSTOM research project represents a complex intervention. The project aim of the intervention is, through the delivery of culturally sensitive Diabetes self-management education and support, to support ethnic minorities with type 2 diabetes in making health-promoting decisions about their care and gaining insight into their goals, values and motivation to improve their daily diabetes self-management. The target group comprises ethnic minorities whose native language is Arabic, Urdu or Turkish.
Detailed Description

The CUSTOM research project represents a complex intervention. The project aim of the intervention is, through the delivery of culturally sensitive DSMES, to support ethnic minorities with type 2 diabetes in making health-promoting decisions about their care and gaining insight into their goals, values and motivation to improve their daily diabetes self-management. The target group comprises ethnic minorities whose native language is Arabic, Urdu or Turkish. The intervention has been developed in collaboration with the target group and health care professionals from Centre for Diabetes (CfD) in Copenhagen Municipality.

CUSTOM will explore feasibility and effectiveness of the intervention including the mechanisms through which outcomes occur and contexts where outcomes are likely to be replicable. The intervention builds on the framework of complex interventions(26), and is designed as an pragmatic randomised controlled trial in three arms.

Focus on fidelity, appropriateness and acceptability of the developed intervention.

  • What factors and structures are necessary to facilitate DSMES access and retention among the target group?
  • Which methods and tools supporting diabetes decision making and problem solving are acceptable and feasible among the target group?
  • What educational strategies promote Health Care Professionals' (HCPs') communication with the target group?

Focus on exploring effectiveness of the intervention, the mechanisms through which outcomes occur and contexts where outcomes are likely to be replicable.

  • To what extent does the intervention lead to better outcomes (e.g., HbA1c and participant-reported outcomes) than 'usual care' for the target group and what mechanisms for the effect of the intervention can be identified? And are there differences according to the setting, of which the intervention is delivered; a) in a community health centre and b) a local community setting.
  • What characterizes contexts that are most conducive to positive outcomes?
  • What barriers and possibilities exist related to implementing culturally sensitive DSMES in different municipal settings targeting ethnic minority groups?
  • Which contextual factors determine whether the identified mechanisms lead to intended outcomes?
  • What are the long-term effects of the intervention on measured outcomes?

Study design CUSTOM is considered a complex intervention due to many interacting components in its design, complex behaviour changes in those delivering and receiving the intervention, many stakeholders, and highly variable outcomes. The trial will be undertaken as a pragmatic trial using cluster randomisation.

The trial will be tested in three arms: Participants will be randomised into 3 arms Group A: Centre for Diabetes, Copenhagen Municipality, n = 103 Group B: Local community setting in Tingbjerg, Copenhagen Municipality, n = 103 Group C: Usual care in the west area of Copenhagen, municipalities of Høje-Taastrup, Hvidovre, Albertslund, Brøndby and Ishøj, n = 103 Figure 1 Study Design 9. Interventions 9.1 Group A and B: Group A and B will receive the same interventions but in different contexts - a local community setting and a diabetes care centre. The intervention will be pilot tested in the local community and if necessary adjusted to local contexts.

Using a design-based research, the intervention has been developed in collaboration with researchers, the target group and healthcare professionals from Centre for Diabetes (CfD) in Copenhagen Municipality.

The group-based course will include 6 sessions of approximately 3 hours. Sessions are constructed around themes such as; diabetes knowledge and complication, mental health, diet, physical activity, Ramadan, medicine and include practical exercises such as blood sugar measurements, walking etc. The healthcare professionals delivering the education consists of an interdisciplinary team of both a nurse, dietitian, physiotherapist, a translator and a peer educator.

The CUSTOM intervention consists of three elements: philosophy/values, educator behaviours and 12 specific dialogue tools. These three elements are all equally important in the organisation and completion of a good and culturally sensitive diabetes education targeting ethnic minorities. The intervention is based on the concept CUSTOM which is developed with regards to the healthcare professionals' approaches, methods and existing educational activities. The concept consists of 12 health education tools accompanied by a comprehensive guide. The success of the tools developed in CUSTOM rely on the values held by the suppliers of the education and by the health care professional's competences to apply the specific dialogue tools.

Study Type Observational
Study Design Not Provided
Target Follow-Up Duration Not Provided
Biospecimen Not Provided
Sampling Method Probability Sample
Study Population Referred to rehabilitation by the GP and has type 2 diabetes
Condition Diabetes Mellitus, Type 2
Intervention Other: Group course
Education and support
Study Groups/Cohorts
  • Intervention, Centre for Diabetes or local setting
    Group-based course in diabetes education including 6 sessions of approximately 3 hours. Sessions are constructed around themes such as; diabetes knowledge and complication, mental health, diet, physical activity, Ramadan, medicine and include practical exercises such as blood sugar measurements, walking etc.
  • Usual care
    Usual care in 5 municipalities in the west area of Copenhagen
    Intervention: Other: Group course
Publications * Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruitment Information
Recruitment Status Recruiting
Estimated Enrollment
 (submitted: May 13, 2019)
309
Original Estimated Enrollment Same as current
Estimated Study Completion Date October 2022
Estimated Primary Completion Date December 31, 2020   (Final data collection date for primary outcome measure)
Eligibility Criteria

Inclusion Criteria:

  • Clinical diagnosis of type 2 diabetes
  • Ability to give written consent
  • Ability and willingness to attend and participate in a group-based education programme.
  • First language is Arabic, Turkish or Urdu.

Exclusion Criteria:

  • Physical illness that could seriously reduce their life expectancy and ability to participate in the trial
  • Mental illness that could reduce their ability to participate in the trial
  • Significant alcohol or substance misuse which could limit the participants ability to participate in the trial
  • A primary diagnosis of learning disability
  • Pregnancy, breastfeeding or plans of pregnancy during the study period
Sex/Gender
Sexes Eligible for Study: All
Ages 18 Years and older   (Adult, Older Adult)
Accepts Healthy Volunteers No
Contacts
Contact: Nana F Hempler, PhD +45 40732591 nana.folmann.hempler@regionh.dk
Contact: Lone B Rasmussen, PhD +45 22857377 lone.banke.rasmussen@regionh.dk
Listed Location Countries Denmark
Removed Location Countries  
 
Administrative Information
NCT Number NCT03950219
Other Study ID Numbers CUSTOM
Has Data Monitoring Committee Yes
U.S. FDA-regulated Product
Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
IPD Sharing Statement Not Provided
Responsible Party Nana Folmann Hempler, Steno Diabetes Center Copenhagen
Study Sponsor Steno Diabetes Center Copenhagen
Collaborators Center for Diabetes, Copenhagen Municipality
Investigators
Principal Investigator: Nana F Hempler, PhD Steno Diabetes Center Copenhagen
PRS Account Steno Diabetes Center Copenhagen
Verification Date October 2020