About this trial

This study will test whether glucose sensor data can be used to identify the time of day when adults with prediabetes are most likely to have high blood sugar after meals. Participants will first wear a continuous glucose monitor and wrist activity monitor and record meal times for 10 days. These data will be used to classify each participant's personal "glycemic vulnerability window," such as morning, evening, or generally variable patterns.

Participants will then be randomly assigned to either personalized meal timing plus a short walk after their most vulnerable meal, or to an attention-matched control group receiving sleep hygiene and general step-count advice. The main outcome will be the change in post-meal glucose exposure during each participant's vulnerable window after 4 weeks.

Eligibility criteria

Qualifiers

Age 30 to 70 years

HbA1c 5.7% to 6.4% within 3 months of screening, or

Fasting plasma glucose 100 to 125 mg/dL on two separate occasions

Body mass index 23 to 40 kg/m²

Disqualifiers

Current or prior diagnosis of type 1 diabetes or type 2 diabetes

Use of glucose-lowering medication within the past 3 months

Use of systemic corticosteroid medication within the past 3 months

Use of prescription weight-loss medication within the past 3 months

Trial design

Treatments tested in this trial

  • Phenotype-Guided Meal Timing and Postprandial Walking
  • Sleep Hygiene and Step-Count Advice

Treatment groups

105 Participants
are divided into 2 treatment groups

Locations

1
Shifa International hospital50, LahoreShaikhupura, Pakistan

Sponsors and collaborators

Shifa International Hospital

Lead sponsor