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NCT Number: NCT03827382

Bicycle Exercise and Lifestyle Intervention in Newly Diagnosed Diabetes

The aim of the study is to test the efficacy, feasibility, and safety of a bicycle exercise followed by an intensive lifestyle intervention for 3 months in patients with recent onset and medically untreated type 2 diabetes.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of Basel, Basel, Canton of Basel-City, Switzerland

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About this study

Lifestyle intervention is a fundamental aspect in the treatment of type 2 diabetes. Implementation of lifestyle changes early after diagnosis often suffices to control metabolic dysregulation and may even have a durable impact. However, implementation of these changes is often difficult for multiple reasons including noncompliance as well as doubt on efficacy of sport and diet changes compared to drugs. Furthermore, most patients with type 2 diabetes remain asymptomatic for a prolonged period of time. Thus, they lack an immediate relief of symptoms and do not feel the benefit of changes in lifestyle. Often, untreated type 2 diabetes first manifests itself with symptoms of polyuria and polydipsia. This offers a unique opportunity to demonstrate the potential of lifestyle changes. However, in daily practice, symptomatic patients with polyuria and polydipsia or with HbA1c levels >10% at diagnosis are typically referred to an emergency room, hospitalized and treated with drugs as a first line treatment.

In the present study, we aim to implement a lifestyle intervention as a first-line treatment in recent onset type 2 diabetes. In the emergency room, the bed will symbolically be removed and the patient requested to perform a bicycle exercise. Non-ER patients will be invited to perform the bicycle exercise as soon as possible. We expect from this educational trigger that patients will realize the therapeutic power of sport. Preliminary interventions using this approach at our emergency room demonstrated the potential of such an intervention. However, internal and external validation, efficacy and safety of a lifestyle intervention in an emergency room remain to be shown in a multi-center controlled study.

The primary endpoint of this study is achievement of metabolic control without anti-diabetic medication 3 months after study enrollment. For the purpose of this study, metabolic control is defined as an HbA1c below a target stratified for three groups according to HbA1c at baseline: HbA1c >14% a target of < 10%; HbA1c < 14% and > 10% a target of < 8%; HbA1c < 10% a target of < 7.5%.

Patients will be randomized either to standard care or to a bicycle exercise followed by an intensive lifestyle intervention on top of non-pharmacological standard care.

After rehydration, patients allocated to the intensified lifestyle intervention group will be instructed to perform 30 minutes of bicycle exercise at 60 % of the calculated maximum heart rate (according to Franckowiak et al.) followed by an intensive lifestyle intervention. Patients will be discharged if the clinical status is stable and no comorbidities require further hospitalization. Follow-up visits at the Clinic of Endocrinology for further instructions and consultation will be carried out after 2, 7, 30, 60 and 90 days, half a year and a year.

In order to monitor blood glucose levels, patients will be instructed on visit 2 to take measurements at home and will be asked to send their fasting glucose levels of the first week to the study team for monitoring of the metabolic situation. This will also be done in the week before visits of day 30 and 90.

The schedule for the intervention arm consists of 3 to 5 aerobic training sessions (duration 15-40 minutes each) and 2 resistance trainings per week, as well as weekly motivational coaching via telephone by the study psychologist. Everyday activity will be objectively monitored using the patient's mobile phone and a blinded actigraph (activity tracker). Exercise sessions will be monitored by weekly phone calls and documented. To assess baseline physical activity all patients will fill in the SIMPAQ questionnaire at baseline and at 6 months.

Measurement of clinical parameters (heart rate, blood pressure), venous blood gas analysis (pH, pCO2, base excess, bicarbonate) at baseline and 120 min after beginning of bicycle exercise. Blood glucose levels at baseline and 30, 60 and 120 min after beginning of bicycle exercise. Blood glucose levels, vital parameters, concomitant medication after 2, 7, 30, 60 and 90 days; HbA1c at baseline, 2 (only intervention group), 3 and 6 months and one year; physical activity at baseline, 3 and 6 months. In the intervention group additional self-measurements of blood glucose levels during the first week and within the week before visit at day 30 and 90 after randomization.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Informed consent as documented by signature
  • Type 2 diabetes diagnosed within the last two years according to the American Diabetes Association (ADA) criteria
  • Age ≥ 18 years
  • HbA1c ≥ 7.5 %

Exclusion criteria

  • Clinically instable patient as defined by the physicians on duty including signs of new cardiac ischemia in the ECG, systolic blood pressure ≥ 200 mmHg, fever ≥ 38.5 °C, symptoms of SIRS or reduced vigilance.
  • Anti-diabetic medication for ≥ 24 hours
  • Inability to perform a bicycle exercise during 30 minutes
  • Previous lifestyle-intervention by an endocrinologist
  • Engagement in physical activity more than five times per week
  • Enrollment in other interventional study

Treatment and study plan

Lifestyle Intervention

Behavioral

Physical activity program: 3-5 aerobic training sessions (15-40 minutes each) per week, combined with 2 resistance training per week as well as motivational coaching via telephone Nutritional counseling

Primary outcomes

  1. metabolic control

    Time frame: 3 months

    fasting glucose < 7.6 mM and HbA1c below a target stratified for three groups according to HbA1c at baseline.

Secondary outcomes

  1. Absolute HbA1c reduction per stratification group

    Time frame: 3 months

    Absolute HbA1c (% points) reduction after 3 months per stratification group (groups consist of HbA1c >14%; HbA1c <14% and >10%; HbA1c <10%)

  2. Absolute HbA1c reduction per stratification group

    Time frame: 6 months

    Absolute HbA1c (% points) reduction after 6 months per stratification group (groups consist of HbA1c >14%; HbA1c <14% and >10%; HbA1c <10%)

  3. Proportion of patients achieving HbA1c target in each stratification group

    Time frame: 3 months

    Proportion (%) of patients achieving target per stratified group after 3 months without anti-diabetic medication other than Metformin (groups consist of HbA1c >14%, HbA1c <14% and >10% and HbA1c <10%)

  4. Feasibility of bicycle exercise at study enrollment in the ER

    Time frame: 2 hours

    Feasibility of bicycle exercise at study enrollment in the ER, defined as absence of problem reports through the study team

  5. Proportion of patients achieving HbA1c target in each stratification group

    Time frame: 6 months

    Proportion (%) of patients achieving target per stratified group after 6 months without anti-diabetic medication other than Metformin (groups consist of HbA1c >14%, HbA1c <14% and >10% and HbA1c <10%)

  6. Changes in heart rate after bicycle intervention

    Time frame: 2 hours

    Changes in heart rate (beats per minute) at the end and 120 min after bicycle exercise in the emergency room compared to baseline

  7. Changes in respiratory rate after bicycle intervention

    Time frame: 2 hours

    Changes in respiratory rate (breaths per minute) at the end and 120 min after bicycle exercise in the emergency room compared to baseline

  8. Changes in blood pressure after bicycle intervention

    Time frame: 2 hours

    Changes in blood pressure (mmHg) at the end and 120 min after bicycle exercise in the emergency room compared to baseline

  9. Changes in blood glucose after bicycle intervention

    Time frame: 2 hours

    Changes in blood glucose (mmol/l) at the end and 120 min after bicycle exercise in the emergency room compared to baseline

  10. Changes in pH after bicycle intervention

    Time frame: 2 hours

    Changes in pH at the end and 120 min after bicycle exercise in the emergency room compared to baseline

  11. Changes in base excess after bicycle intervention

    Time frame: 2 hours

    Changes in base excess (BE) at the end and 120 min after bicycle exercise in the emergency room compared to baseline

  12. Changes in bicarbonate after bicycle intervention

    Time frame: 2 hours

    Changes in bicarbonate (mmol/l) at the end and 120 min after bicycle exercise in the emergency room compared to baseline

  13. Incidence of exercise related Adverse Events (Safety) during bicycle exercise in the ER

    Time frame: 2 hours

    Incidence of exercise related Adverse Events (cardiac, circulatory, pulmonary, neurologic complications) during bicycle exercise after diabetes diagnosis in the ER

  14. Incidence of Treatment-Emergent Adverse Events (Safety and Tolerability)

    Time frame: 6 months

    Incidence of Treatment-Emergent Adverse Events (Safety and Tolerability) during intensive lifestyle intervention after new diagnosis of type 2 diabetes

  15. Re-hospitalization rate

    Time frame: 3 months

    Re-hospitalizations within 3 months after discharge from the emergency room.

  16. Re-consultation rate

    Time frame: 3 months

    Rate of unplanned re-consultations within 3 months after discharge from the emergency room.

  17. Changes in HbA1c at 6 months

    Time frame: 6 months

    Changes in HbA1c (in % points) at 6 months compared to baseline assessed by blood sample

  18. Changes in physical activity at 6 months

    Time frame: 6 months

    Changes in physical activity at 6 months compared to baseline assessed by SIMPAQ questionnaire and actigraph.

    The SIMPAQ (Simple Physical Activity Questionnaire) measures daily physical activity. Time spent sedentary and active is measured in hours per day.

  19. Number of antidiabetic medication at 30 days

    Time frame: 30 days

    Number of antidiabetic medication at 30 compared to baseline in both arms

  20. Number of antidiabetic medication 60 days

    Time frame: 60 days

    Number of antidiabetic medication 60 days compared to baseline in both arms

  21. Number of antidiabetic medication at 90 days

    Time frame: 90 months

    Number of antidiabetic medication at 90 days compared to baseline in both arms

  22. Dosage of antidiabetic medication at 30

    Time frame: 30 days

    Dosage of antidiabetic medication at 30 days compared to baseline in both arms

  23. Dosage of antidiabetic medication at 60 days

    Time frame: 60 days

    Dosage of antidiabetic medication at 60 days compared to baseline in both arms

  24. Dosage of antidiabetic medication at 90 days

    Time frame: 90 days

    Dosage of antidiabetic medication at 90 days compared to baseline in both arms

  25. Quality of life by SF-36 Questionnaire

    Time frame: 6 months

    Quality of life at 6 months in intervention group as compared to standard of care as assessed by SF-36 questionnaire. The Short Form (36) Health Survey is a 36-item, patient-reported survey of patient health. The SF-36 consists of eight scaled scores, which are the weighted sums of the questions in their section. Each scale is directly transformed into a 0-100 scale on the assumption that each question carries equal weight. The lower the score the more disability. The higher the score the less disability i.e., a score of zero is equivalent to maximum disability and a score of 100 is equivalent to no disability.

Study contacts

Contact information is provided by the study sponsor or research team.

Marc Y Donath, Prof.

CONTACT

[email protected]

0041 61 265 50 78

Matthias Hepprich, MD

CONTACT

[email protected]

0041 61 328 60 77

Sponsors and collaborators

Lead sponsor

University Hospital, Basel, Switzerland

Other

Collaborators

  • Kantonsspital Olten

Registry information

Acronym: BELIFE

Important dates

Study start
2019
Primary completion
2025
Study completion
2025
First posted
Feb 1, 2019
Registry last updated
Feb 14, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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