SSRD and Overweight

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-70
SponsorRegion Skane

About this trial

The investigators have previously found that a starch- and sucrosereduced diet (SSRD) has led decreased gastrointestinal symptoms in patients with irritabel bowel syndrome (IBS). At the same time, investigators found that the weight was reduced and the nutrient intake was improved with a more favorable metabolic profile. However, it is a challenge to change lifestyle, and most persons fail to keep on with an improved diet for a long time. Investigators therefore now want to conduct a clinical trial with SSRD in overweight/obesity for 3 months. Persons with a BMI \>25 kg/m2 will be included. To examine whether a feedback about improved metabolic profile enhances the compliance, participants will be randomized to be informed or not about the metabolic profile after the 6-week visit. Investigator´s hypothesis is that information about the improvement in the metabolic profile should increase the motivation and compliance in the patients, and thereby render better effects.

Eligibility criteria

Qualifiers

Ålder 18-70 år och språkkunskaper i svenska så att de kan tillgodogöra sig kostinformationen och ifylla formulären.

BMI ≥25 kg/m2

Disqualifiers

Allvarlig födoämnesallergi

Allvarlig hjärt, lung, kardiovaskulär, magtarm, malign eller psykisk sjukdom

Pågående ätstörning

Graviditet

Trial design

Treatments tested in this trial

  • Dietary intervention with SSRD in combination with feedback information about the metabolic profile
  • Dietary intervention with SSRD without any feedback on metabolic profile

Treatment groups

300 Participants
are divided into 2 treatment groups

Locations

This trial has no locations

Sponsors and collaborators