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Co-designing a Pacific diabetes prevention program with families and communities

Effect of a co-designed Pacific diabetes prevention program for improving the health and wellbeing of families and communities

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12621000806864
Acronym
F-DIP
Enrollment
100
Registered
2021-06-25
Start date
2021-07-27
Completion date
2021-08-09
Last updated
2021-11-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

The distribution of and access to resources to enable better health and wellbeing for Pacific families with members who have long-term conditions, continues to be unequal, and lacks cultural responsiveness that is acceptable to Pacific groups living in hard to reach regions. This project uses a co-design approach, and the central research questions are: Is a family-centered diabetes intervention programme for Pacific families an effective approach to prevent diabetes? The impact of the overall research programme will provide a methodological approach that can be replicated in other communities and ethnic groups.

Interventions

Participants with a recently diagnosed prediabetes and/or diabetes (defined by having an HbA1c test in the last 12 months) will be invited to join the study from Phase 1 of the study, that focuses on co-designing the intervention programme. The co-design programme will be delivered to the community over a 24 week period, every week for up to 2 hours per meeting. These co-design meetings will be conducted in face-to-face workshops, delivered by the Community Coordinator (who is already trained

Participants with a recently diagnosed prediabetes and/or diabetes (defined by having an HbA1c test in the last 12 months) will be invited to join the study from Phase 1 of the study, that focuses on co-designing the intervention programme. The co-design programme will be delivered to the community over a 24 week period, every week for up to 2 hours per meeting. These co-design meetings will be conducted in face-to-face workshops, delivered by the Community Coordinator (who is already trained in the co-design methodology). Phase 2 study participants include the same participants with prediabetes/diabetes diagnosis from phase 1, and their families (approximately 100 individuals >18years old). It is anticipated that the co-designed life-style based and behavioural change intervention programme may include weekly activities, such as increased physical activities (eg. organised community 4km walks, community-based fitness classes), and behavioural change activities (eg. educational modules related to cooking and nutritional skills). The intervention programme will be measured at baseline (time-point 1: week 0) and at post-intervention (time-point 2: week 24). Data collection at Time-point 1: • Socio-demographic data: date of birth, gender, ethnicity, highest education level, and annual household income; • Anthropometry: self-reported weight (kilograms) and height (centimetres); blood pressure; diet diversity • Health status: self-reported health condition(s) defined as being told by a doctor that they have this condition, including prediabetes, diabetes, and heart disease; • Holistic wellbeing (for Pasifika participants): spiritual, physical, mental and family wellbeing measured by 10-items based on the Fonofale Model. All answers are measured on a 5-point Likert scale. Data collection at Time-point 2: Anthropometry: self-reported weight (kilograms) and height (centimetres); blood pressure; diet diversity • Health status: self-reported health condition(s) defined as being told by a doctor that they have this condition, including prediabetes, diabetes, and heart disease; • Holistic wellbeing (for Pasifika participants): spiritual, physical, mental and family wellbeing measured by 10-items based on the Fonofale Model. All answers are measured on a 5-point Likert scale.

Sponsors

Massey University
Lead SponsorUniversity

Study design

Allocation
Non-randomised trial
Intervention model
Single group
Primary purpose
Prevention
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

The inclusion criteria: Pacific ethnicity (self-identified), with at least one family member at high risk of developing diabetes (defined by having a BMI>30 and high blood-pressure) and resides in a moderate-high deprivation area.

Exclusion criteria

Non-Pacific participants; Has had chronic diabetes and have had medical complications related to diabetes longer than 12months; Has not been amendable to previous interventions offered (ie. non-compliant).

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026