Evidence map›Paper›PMID 27421729›Full record

Trial reportDiabetologia2016

Effects of exercise training alone vs a combined exercise and nutritional lifestyle intervention on glucose homeostasis in prediabetic individuals: a randomised controlled trial.

Cris A Slentz, Lori A Bateman, Leslie H Willis, Esther O Granville, Lucy W Piner, Gregory P Samsa, Tracy L Setji, Michael J Muehlbauer, Kim M Huffman, Connie W Bales and 1 more

Registry-linked trialOpen access · bronzeAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Diabetologia, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00962962 (Exercise Dose-Response Effects in Prediabetes), which is not on this map. Cited by 77 papers, 9 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
77citing papers in PubMed, 9 pooled it
9.7field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT00962962 nacompletednot on this map

Exercise Dose-Response Effects in Prediabetes: Responses and Mechanisms

TypeinterventionalSponsorDuke UniversityRan2009 to 2013Enrolled288ConditionsPre-DiabetesArmsAerobic Exercise, Exercise and Diet
3 · Its place in the literature

Who cites it

77 citing papers in PubMed, 9 syntheses or guidelines pooled it, 128 citations in OpenAlex.

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  6. American Association of Clinical Endocrinology Clinical Practice Guideline: Developing a Diabetes Mellitus Comprehensive Care Plan-2022 Update.Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists · 2022
    Guideline
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17 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 1 institution in 1 country.

Cris A SlentzDuke Molecular Physiology Institute, Department of Medicine, Duke University School of Medicine, 300 North Duke Street, Durham, NC, 27701, USA. cris.slentz@duke.edu.
Lori A BatemanDuke Molecular Physiology Institute, Department of Medicine, Duke University School of Medicine, 300 North Duke Street, Durham, NC, 27701, USA.
Leslie H WillisDuke Molecular Physiology Institute, Department of Medicine, Duke University School of Medicine, 300 North Duke Street, Durham, NC, 27701, USA.
Esther O GranvilleDivision of Geriatrics, Duke University School of Medicine, Durham, NC, USA.
Lucy W PinerDuke Molecular Physiology Institute, Department of Medicine, Duke University School of Medicine, 300 North Duke Street, Durham, NC, 27701, USA.
Gregory P SamsaDepartment of Biostatistics and Bioinformatics, Duke University School of Medicine, Durham, NC, USA.
Tracy L SetjiDivision of Endocrinology, Duke University School of Medicine, Durham, NC, USA.
Michael J MuehlbauerDuke Molecular Physiology Institute, Department of Medicine, Duke University School of Medicine, 300 North Duke Street, Durham, NC, 27701, USA.
Kim M HuffmanDuke Molecular Physiology Institute, Department of Medicine, Duke University School of Medicine, 300 North Duke Street, Durham, NC, 27701, USA.
Connie W BalesDivision of Geriatrics, Duke University School of Medicine, Durham, NC, USA.
William E KrausDuke Molecular Physiology Institute, Department of Medicine, Duke University School of Medicine, 300 North Duke Street, Durham, NC, 27701, USA.
Duke University · US

Funding

Exercise Dose-Response Effects in Prediabetes:Responses and MechanismsR01DK081559 · NIDDK · DUKE UNIVERSITY · PI KRAUS, WILLIAM E · 2009 to 2013
$3.1M
NIDDK NIH HHS R01 DK081559
6 · The paper itself

Abstract

aims/hypothesisAlthough the Diabetes Prevention Program (DPP) established lifestyle changes (diet, exercise and weight loss) as the 'gold standard' preventive therapy for diabetes, the relative contribution of exercise alone to the overall utility of the combined diet and exercise effect of DPP is unknown; furthermore, the optimal intensity of exercise for preventing progression to diabetes remains very controversial. To establish clinical efficacy, we undertook a study (2009 to 2013) to determine: how much of the effect on measures of glucose homeostasis of a 6 month programme modelled after the first 6 months of the DPP is due to exercise alone; whether moderate- or vigorous-intensity exercise is better for improving glucose homeostasis; and to what extent amount of exercise is a contributor to improving glucose control. The primary outcome was improvement in fasting plasma glucose, with improvement in plasma glucose AUC response to an OGTT as the major secondary outcome.

methodsThe trial was a parallel clinical trial. Sedentary, non-smokers who were 45-75 year old adults (n = 237) with elevated fasting glucose (5.28-6.94 mmol/l) but without cardiovascular disease, uncontrolled hypertension, or diabetes, from the Durham area, were studied at Duke University. They were randomised into one of four 6 month interventions: (1) low amount (42 kJ kg body weight(-1) week(-1) [KKW])/moderate intensity: equivalent of expending 42 KKW (e.g. walking ∼16 km [8.6 miles] per week) with moderate-intensity (50% [Formula: see text]) exercise; (2) high amount (67 KKW)/moderate intensity: equivalent of expending 67 KKW (∼22.3 km [13.8 miles] per week) with moderate-intensity exercise; (3) high amount (67 KKW)/vigorous intensity: equivalent to group 2, but with vigorous-intensity exercise (75% [Formula: see text]); and (4) diet + 42 KKW moderate intensity: same as group 1 but with diet and weight loss (7%) to mimic the first 6 months of the DPP. Computer-generated randomisation lists were provided by our statistician (G. P. Samsa). The randomisation list was maintained by L. H. Willis and C. A. Slentz with no knowledge of or input into the scheduling, whereas all scheduling was done by L. A. Bateman, with no knowledge of the randomisation list. Subjects were automatically assigned to the next group listed on the randomisation sheet (with no ability to manipulate the list order) on the day that they came in for the OGTT, by L. H. Willis. All plasma analysis was done blinded by the individuals doing the measurements (i.e. lipids, glucose, insulin). Subjects and research staff (other than individuals analysing the blood) were not blinded to the group assignments.

resultsNumber randomised, completers and number analysed with complete OGTT data for each group were: low-amount/moderate-intensity (61, 43, 35); high-amount/moderate-intensity (61, 44, 40); high-amount/vigorous-intensity (61, 43, 38); diet/exercise (54, 45, 37), respectively. Only the diet and exercise group experienced a decrease in fasting glucose (p < 0.001). The means and 95% CIs for changes in fasting glucose (mmol/l) for each group were: high-amount/moderate-intensity -0.07 (-0.20, 0.06); high-amount/vigorous 0.06 (-0.07, 0.19); low-amount/moderate 0.05 (-0.05, 0.15); and diet/exercise -0.32 (-0.46, -0.18). The effects sizes for each group (in the same order) were: 0.17, 0.15, 0.18 and 0.71, respecively. For glucose tolerance (glucose AUC of OGTT), similar improvements were observed for the diet and exercise (8.2% improvement, effect size 0.73) and the 67 KKW moderate-intensity exercise (6.4% improvement, effect size 0.60) groups; moderate-intensity exercise was significantly more effective than the same amount of vigorous-intensity exercise (p < 0.0207). The equivalent amount of vigorous-intensity exercise alone did not significantly improve glucose tolerance (1.2% improvement, effect size 0.21). Changes in insulin AUC, fasting plasma glucose and insulin did not differ among the exercise groups and were numerically inferior to the diet and exercise group. CONCLUSIONS/

interpretationIn the present clinical efficacy trial we found that a high amount of moderate-intensity exercise alone was very effective at improving oral glucose tolerance despite a relatively modest 2 kg change in body fat mass. These data, combined with numerous published observations of the strong independent relation between postprandial glucose concentrations and prediction of future diabetes, suggest that walking ∼18.2 km (22.3 km prescribed with 81.6% adherence in the 67 KKW moderate-intensity group) per week may be nearly as effective as a more intensive multicomponent approach involving diet, exercise and weight loss for preventing the progression to diabetes in prediabetic individuals. These findings have important implications for the choice of clinical intervention to prevent progression to type 2 diabetes for those at high risk.

trial registrationClinicalTrials.gov NCT00962962

fundingThe study was funded by National Institutes for Health National Institute of Diabetes and Digestive and Kidney Diseases (NIH-NDDK) (R01DK081559).

Indexed as

AgedBlood GlucoseDiabetes Mellitus, Type 2ExerciseFemaleGlucose Tolerance TestHomeostasisHumansInsulinLife StyleMaleMiddle AgedPrediabetic StateWeight LossBlood GlucoseInsulinDiabetes Prevention ProgramExercise intensityGlucose toleranceImpaired fasting glucoseInsulin sensitivityWeight-loss diet

Identifiers

PMID27421729
PMCPMC5026926
OpenAlexW2464450741

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.