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

Diabetes Mellitus, Type 2 Clinical Trial

— CUSTOM  

Official title:

CUlturally Sensitive TOols and Methods for Ethnic Minorities (CUSTOM): Building Bridges Between Theory and Practice in Diabetes Self-management Education and Support

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT03950219
• Other study ID #: CUSTOM
• Status: Recruiting
• Start date: March 1, 2019
• Est. completion date: October 2022

Study information

• Verified date: October 2020
• Source: Steno Diabetes Center Copenhagen
• Contact: Nana F Hempler, PhD
• Phone: +45 40732591
• Email: nana.folmann.hempler[@]regionh.dk
• Is FDA regulated: No
• Study type: Observational

Clinical Trial 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.

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.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 309
• Est. completion date: October 2022
• Est. primary completion date: December 31, 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

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

Related Conditions & MeSH terms

• Diabetes Mellitus
• Diabetes Mellitus, Type 2

Intervention

Other:
• Group course
Education and support

Locations

Country	Name	City	State
Denmark	Centre for Diabetes	Copenhagen

Sponsors (2)

Lead Sponsor	Collaborator
Steno Diabetes Center Copenhagen	Centre for Diabetes, Copenhagen municipality

Country where clinical trial is conducted

Denmark, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Well-being	questionnaire	6 months
Primary	diabetes self-management	questionnaire	6 months
Primary	HbA1c	blood sample	6 months