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Effectiveness of an Online Self-management Intervention for Type 2 Diabetes Mellitus

Not Applicable
Withdrawn
Conditions
Type 2 Diabetes
Interventions
Behavioral: covivio (additional to treatment as usual)
Other: treatment as usual
Registration Number
NCT05525117
Lead Sponsor
Gaia AG
Brief Summary

This trial was designed to evaluate the effectiveness of the dialogue-based online intervention covivio, which was designed to improve diabetes self-management in patients with type 2 diabetes.

The study aims to test the hypothesis that covivio has a greater positive impact on glycemic control than treatment as usual. Patients with type 2 diabetes mellitus will be randomized and allocated to either an intervention group, receiving covivio in addition to treatment as usual, or a control group, which receives only treatment as usual. The primary endpoint is the HbA1c value six month after baseline.

Detailed Description

The aim of this clinical trial is to investigate the effectiveness of the self-guided digital therapeutic covivio in 268 patients with type 2 diabetes mellitus (T2DM). Patients will be randomized and allocated in a 1:1 ratio to either an intervention group, in which they will receive access to covivio in addition to treatment as usual (TAU, n = 134), or to a control group, in which they will receive only TAU (n = 134).

The primary endpoint of this trial will be the between-groups difference of the HbA1c in the intervention and control group at six months adjusted for the baseline HbA1c. In order to show the course of change over time, two timepoints for assessment of effects are planned at four (T1) and six months (T2) after the baseline assessment (T0). The primary endpoint will be the HbA1c at six months post-allocation. Secondary endpoints will be depression, diabetes self-management (DSM), BMI, and quality of life. Figure 1 (section 6.1) summarizes the design of the clinical trial.

Recruitment & Eligibility

Status
WITHDRAWN
Sex
All
Target Recruitment
Not specified
Inclusion Criteria
  • diagnosis of T2DM (submission of a medical certificate attesting to the presence of at least one of the following ICD-10-GM diagnoses of T2DM: E11.20, E11.30, E11.40, E11.50, E11.60, E11.72, E11.74, E11.80, E11.90)
  • HbA1c value ≥ 7.0% (53 mmol/mol)
  • BMI ≥ 23 kg/m2
  • Consent to participate
  • Sufficient knowledge of the German language
Exclusion Criteria
  • diagnosis of type 1 diabetes mellitus (T1DM)
  • change in medication, frequency of use or dosage (planned within 4 weeks before T0 or during the study period)

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
online intervention in addition to treatment-as-usualcovivio (additional to treatment as usual)online intervention: covivio in addition to treatment as usual
treatment-as-usualtreatment as usualOther: treatment as usual
Primary Outcome Measures
NameTimeMethod
HbA1c6 months

The primary objective of this study is to determine whether the online intervention covivio will reduce HbA1c values in the intervention group compared to the control group.

Secondary Outcome Measures
NameTimeMethod
Diabetes Self-management6 months

assessed with the total mean score of the Diabetes Self-management questionnaire (DSMQ)

Body Mass Index6 months

calculated from measurement data of patient's height in meter and weight in kilogram

Depressive symptoms6 months

assessed with the total score of the Patient Health Questionnaire (PHQ-9)

Health-Related Quality of Life6 months

assessed with the total score of the Assessment of Quality of Life (AQoL-8D)

Proportion of patients achieving a reduction in HbA1c6 months

A reduction of HbA1c values by at least 0.3% from baseline to T2 will be considered a significant clinical improvement in glycemic control

Trial Locations

Locations (1)

GAIA

🇩🇪

Hamburg, Germany

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