Evidence map›Paper›PMID 27394386›Full record

Trial reportContemporary clinical trials2016

Prepare, a randomized trial to promote and evaluate weight loss among overweight and obese women planning pregnancy: Study design and rationale.

Erin S LeBlanc, Kimberly K Vesco, Kristine L Funk, Njeri Karanja, Ning Smith, Victor J Stevens

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Contemporary clinical trials, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
0.7field-weighted citation impact, top 25% 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 12 citations in OpenAlex.

  1. Pooled it
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  6. Article
  7. Review
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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

6 authors at 1 institution in 1 country.

Erin S LeBlancCenter for Health Research, Kaiser Permanente Northwest, 3800 N. Interstate Ave, Portland, OR 97227, USA. Electronic address: Erin.S.LeBlanc@kpchr.org.
Kimberly K VescoCenter for Health Research, Kaiser Permanente Northwest, 3800 N. Interstate Ave, Portland, OR 97227, USA. Electronic address: Kimberly.K.Vesco@kpchr.org.
Kristine L FunkCenter for Health Research, Kaiser Permanente Northwest, 3800 N. Interstate Ave, Portland, OR 97227, USA. Electronic address: Kristine.Funk@kpchr.org.
Njeri KaranjaCenter for Health Research, Kaiser Permanente Northwest, 3800 N. Interstate Ave, Portland, OR 97227, USA. Electronic address: Njeri.Karanja@kpchr.org.
Ning SmithCenter for Health Research, Kaiser Permanente Northwest, 3800 N. Interstate Ave, Portland, OR 97227, USA. Electronic address: Ning.X.Smith@kpchr.org.
Victor J StevensCenter for Health Research, Kaiser Permanente Northwest, 3800 N. Interstate Ave, Portland, OR 97227, USA. Electronic address: Victor.J.Stevens@kpchr.org.
Kaiser Permanente Center for Health Research · US

Funding

PREPARE: A randomized trial of a pre-pregnancy weight loss interventionR01DK099882 · NIDDK · KAISER FOUNDATION RESEARCH INSTITUTE · PI LEBLANC, ERIN S · 2014 to 2017
$2.8M
PREPARE OS: An observational study of mother-offspring dyads from a randomized trial of a prepregnancy weight loss interventionR56DK099882 · NIDDK · KAISER FOUNDATION RESEARCH INSTITUTE · PI LEBLANC, ERIN S · 2018 to 2018
$426k
NIDDK NIH HHS R01 DK099882NIDDK NIH HHS R56 DK099882
6 · The paper itself

Abstract

backgroundWomen who are overweight or have obesity at pregnancy onset, and those who gain excessive weight during pregnancy, are at increased risk of pregnancy-related complications and large for gestational age infants.

objectiveThis report describes methodology for the Prepare study, a randomized, controlled clinical trial testing a preconception and pregnancy weight management program for women who are overweight or have obesity (BMI≥27kg/m(2)). OUTCOMES: This trial examines multiple pregnancy and neonatal outcomes, with the primary outcome being gestational weight gain (GWG). Secondary outcomes include change in weight before conception, offspring birth weight adjusted for gestational age, offspring weight for length, and pregnancy diet quality and physical activity level.

methodsNonpregnant women who anticipate becoming pregnant in the next 2years are randomly assigned to an intervention program or a usual care control condition. Intervention participants receive weight management counseling by telephone before and during pregnancy, with weekly contacts during the first 6months and monthly contacts for the next 18months. Intervention participants also have unlimited access to a study website that provides self-management tools. All participants who become pregnant are contacted at 20weeks' gestation to assess physical activity levels and dietary habits. All other outcome data are obtained from medical records. Intervention satisfaction is assessed via questionnaire. SUMMARY: This clinical trial tests the efficacy of an intervention program designed to help overweight and obese women achieve healthy lifestyle changes that will result in a healthy weight prior to pregnancy and appropriate weight gain during pregnancy.

Indexed as

Weight Reduction ProgramsAdultFemaleFetal MacrosomiaHumansObesityOverweightPreconception CarePregnancyPregnancy ComplicationsPrenatal CareWeight GainPregnancyPrenatalWeight loss

Identifiers

PMID27394386
PMCPMC5685182
OpenAlexW2464811152

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.