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N/A N=54 Randomized Single-blind Basic Science

Effects of Breaking up Prolonged Sitting on Postprandial Cardiometabolic Disease Risk Markers in South Asian Adults

Cardiovascular Risk Factor · Cardiovascular Diseases · Diabetes · Physical Activity · Sedentary Lifestyle

Enrolled (actual)
54
Serious AEs
0.0%
Results posted
Apr 2026
Primary outcome: Primary: Postprandial Glucose — 1.46; 1.43; 1.74; 1.53 mmol.L-1.5 h-1

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Breaking up sitting with walking breaks (INT-SIT) (Other); Prolonged sitting (SIT) (Other)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
University of Bedfordshire
Primary completion
Mar 2020

Outcome Measures

OutcomeResultp-value
PRIMARY
Postprandial Glucose
1.46; 1.43; 1.74; 1.53
SECONDARY
Postprandial Triglycerides
0.35; 0.23; 0.67; 0.63
SECONDARY
Postprandial Insulin
24.69; 26.95; 44.19; 41.12
SECONDARY
Metabolic Load Index
1.76; 1.60; 2.39; 2.17
SECONDARY
Resting Energy Expenditure
0.22; 0.21; 0.18; 0.23
SECONDARY
Resting Fat Oxidation
3.21; 0.67; 2.42; 2.12
SECONDARY
Resting Carbohydrate Oxidation
44.28; 54.75; 43.57; 52.38
SECONDARY
Mean Arterial Pressure
89.17; 87.24; 94.22; 93.33
SECONDARY
Heart Rate
67.50; 67.62; 69.24; 69.76

Summary

The purpose of this study is to examine whether breaking up prolonged sitting with short regular bouts of walking can reduce blood sugar and cholesterol levels after eating, which are risk markers for Type 2 diabetes and heart disease. This study will compare these responses in normal-weight versus overweight/obese South Asian adults.

Eligibility Criteria

Inclusion Criteria

  • Self-identified South Asian ethnicity.
  • Self-report sitting at least 7 hours per day.
  • Normal weight, overweight or obese.

Exclusion Criteria

  • Unable to speak and read English.
  • Contraindications to performing light-intensity walking.
  • Diagnosed cardiovascular disease or diabetes.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT03898206). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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