Development and evaluation of lifestyle interventions for patients with pre-diabetes
- Conditions
- Pre-diabetesMetabolic and Endocrine - Diabetes
- Registration Number
- ACTRN12619001374156
- Lead Sponsor
- Massey University Psychology Department, Palmerston North
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 87
Inclusion criteria required that patients were:
1. Over the age of 18
2. Fluent in spoken and written English
3. Had a formal classification of pre-diabetes from a registered medical professional.
The prediabetes inclusion criteria were based on World Health Organisation (WHO) criteria for pre-diabetes classification. This requires patients to have an impaired fasting glucose (IFG between 6.1 and 6.9 mmol-1 inclusive) and an impaired glucose tolerance (IGT 2 hour postprandial glucose concentration between 7.8 and 11 mmol), and/or an HbA1c between 41 and 49.
1. Cognitively impaired.
2. At risk of harm to/from themselves or others (i.e., suicidal/homicidal ideation).
3. Comorbid medical diagnosis or condition that is terminal and likely to be fatal within one year.
4. Already participating in a formal pre-diabetes lifestyle education intervention.
5. Receiving psychiatric or psychological intervention at the time of recruitment or has a severe psychiatric disorder (e.g., schizophrenia).
6. Meets criteria for type 2 diabetes. Again, this is based on WHO criteria (i.e., IFG greater than or equal to 7mmol/l, and/or 2-hour plasma glucose of greater than or equal to 11.1 mmol/l and/or HbA1c of 50 mmol/l or greater).
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method