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Testing the effectiveness of a mindfulness-based intervention to reduce distress in people with diabetes

Testing the effectiveness of a mindfulness-based intervention to reduce distress in people with diabetes: A pilot study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12613000898752
Acronym
None
Enrollment
100
Registered
2013-08-12
Start date
2013-08-07
Completion date
Unknown
Last updated
2024-12-09

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

Conditions

None listed

Brief summary

Mindfulness-based intervention programs are a promising intervention in the treatment of psychological distress in a range of clinical populations including pain disorders, cancer and other medical problems. There is, however a paucity of studies that have examined mindfulness in people with diabetes. The few studies that have been undertaken have shown the intervention to result in improvements in emotional well-being (anxiety and depression), improved self-care behaviours and decreased HbA1c values. This study will assess the effects of a mindfulness-based intervention undertaken and self-directed in people with diabetes at home over an eight-week period. This study will seek to determine whether a mindfulness-intervention undertaken in the patients’ home can: Reduce anxiety and depression Reduce perceived diabetes –specific stress Improve diabetes self-care and management Improve glycemic control (HbA1c) Increase mindfulness strategies (acceptance and action) in relation to diabetes

Interventions

A CD of guided mindfulness practice to be performed each day for 8 weeks at home. The duration of the daily practice is 30 minutes and participants are required to fill in a daily practice record. The intervention CD consists of a fully guided mindfulness session about the process of placing your attention on your breath. It is the same each day.

Sponsors

Dr Sue Pearson
Lead SponsorIndividual

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Open (masking not used)

Eligibility

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

Inclusion criteria

Type 2 diabetes

Exclusion criteria

Current regular practice of mindfulness Recent history of severe psychopathology Insufficient reading or comprehension skills or incapable of signing the informed consent A K10 score > 30

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026