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Depressive symptoms, sleep quality and cognitive functioning in outpatients with type 2 diabetes

Depressive symptoms, sleep quality and cognitive functioning in outpatients with type 2 diabetes - Depressive symptoms, sleep quality and cognitive functioning in diabetics

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON41784
Enrollment
50
Registered
2015-02-26
Start date
2015-02-01
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

Diabetes mellitus sugar diabetes

Interventions

cognition
depression
diabetes
sleep

Sponsors

Universiteit van Tilburg
Lead Sponsor

Eligibility

Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria for this study are patients with diabetes type 2 between 55 and 80 years of age. Participants need to have a minimal diabetes duration of one year, need to be functionally independent and capable of understanding the Dutch language. Since comorbidity is a part of the diabetic condition, participants with diabetes-related conditions will be included.

Exclusion criteria

Exclusion criteria: Exclusion criteria are a history of alcohol or substance abuse and all other psychiatric or neurological disorders.

Design outcomes

Primary

MeasureTime frame
- Cognitive functioning will be measured in three domains; memory, information-processing speed and attention & executive functioning o Memory * Rey cft * 15 woordentest * Digit span WAIS-IV-NL o Information-processing speed * TMT-A * Stroop part 1 & 2 o Attention & executive functioning * TMT-B * Stroop part 3 * Letter fluency * Modified Wisconsin cart sorting task - Depressive symptoms will be measured the PHQ-9 questionnaire. - Sleep quality will be measured with the Pittsburgh sleep quality index.

Secondary

MeasureTime frame
The following factors will be measured and analysed: HbA1c, Blood pressure, Cholesterol, Any macrovascular event, Diabetes duration, History of hypertension, Hypoglycemic events, Stroke or cardiovascular disease. The following factors will be measured because they might intervene with the study parameters: Medication use, Smoking and alcohol consumption habits, BMI, Head trauma.

Countries

The Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)