Skip to main content
Clinical Trials/NCT03090074
NCT03090074
Unknown
Not Applicable

To Lower Glucose Levels and Reduce Weight by Exclusion of Carbohydrates and Inclusion of Psychological Behavioral Support

University Hospital, Linkoeping1 site in 1 country200 target enrollmentMarch 20, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Glucose Metabolism Disorders
Sponsor
University Hospital, Linkoeping
Enrollment
200
Locations
1
Primary Endpoint
Long-term glucose levels
Last Updated
6 years ago

Overview

Brief Summary

Risk-patients for diabetes or patients that are diagnosed with this condition but who are not treated with insulin are randomized two times, according to diet and according to the type of support:

Randomization with regard to carbohydrate restriction (25-30 E% or < 10E%). Randomization with regard to type of psychological support. Either according to Acceptance and Commitment Therapy or to traditional cognitive behavioral therapy. Both kinds of psychological support is given as group therapy.

Two-hundred patients are recruited and each patient is followed for two years.

Detailed Description

The organizers will recruit 200 patients in the study "To lower glucose levels and reduce weight by exclusion of carbohydrates and inclusion of psychological behavioral support" (LOWinCHIP) at the primary care health center "Cithyhälsan Centrum" in Norrköping. Each patient will be followed for 2 years. Patients are eligible if they have are above 18 years of age and have a BMI above 28 kg/m2 and also belong to one or more of the following groups: 1) type 2 diabetes that is not treated with insulin. 2) Patients that have had gestational diabetes or who have 3) first grade relative with type 2 diabetes. Finally 4) pre-diabetic individuals with impaired fasting glucose (6.1-6.9 mmol) or impaired glucose tolerance (capillary plasma glucose 8.9-12-1 after glucose challenge) are also potential participants. Patients must not have insulin therapy or severe kidney failure (GFR\< 30). They can also not have severe physical restrictions for activity and they must not have difficulties with understanding written Swedish texts. The participants are randomized two times (two by two factorial): Randomization with regard to carbohydrate restriction (25-30 E% or \< 10E%). Randomization with regard to type of psychological support. Either according to Acceptance and Commitment Therapy (ACT) or to traditional cognitive behavioral therapy. Each group will have three group sessions with approximately 8 participants followed by a telephone call by the therapist. Each session will be held by the psychologists that are part of the Cityhälsan Centrum staff. The study has \> 95% power to demonstrate 5% HbA1c (mmol/mol) difference between groups with a drop out of 25%.

Registry
clinicaltrials.gov
Start Date
March 20, 2017
End Date
March 19, 2021
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
University Hospital, Linkoeping
Responsible Party
Principal Investigator
Principal Investigator

Fredrik H Nystrom

Professor, head of Internal Medicine, consultant in Endocrinology.

University Hospital, Linkoeping

Eligibility Criteria

Inclusion Criteria

  • Diabetes without insulin. Patients at high risk for developing diabetes.

Exclusion Criteria

  • Severe kidney failure. Insulin therapy. Inability to understand instructions.

Outcomes

Primary Outcomes

Long-term glucose levels

Time Frame: 2 years

HbA1c levels

Secondary Outcomes

  • Cardiovascular risk factors(2 years)
  • Quality of Life(2 years)

Study Sites (1)

Loading locations...

Similar Trials