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Clinical Trials/NCT06157684
NCT06157684RecruitingNot Applicable

Assessment of the Effect of Postprandial Ambulation on Birth Weight Percentile in Patients With Gestational Diabetes Mellitus.

Women and Infants Hospital of Rhode Island1 site in 1 country90 target enrollmentStarted: October 1, 2022Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Sponsor
Enrollment
90
Locations
1
Primary Endpoint
Infant birthweight percentile

Study Overview

Brief Summary

This is a randomized controlled trial to assess the effect of routine exercise counseling compared to the recommendation for postprandial ambulation on infant birthweight among pregnant people with gestational diabetes mellitus.

The primary outcome is birthweight percentile for gestational age at delivery.

Secondary outcomes include feasibility and acceptability, need for metformin or insulin for glycemic control, mode of delivery, neonatal hypoglycemia.

Participants will be counseled to either complete 20 minutes of walking after meals, or be counseled with routine exercise counseling of 30 minutes of low-impact 5x a week. Their activity will be tracked by "FitBit" pedometers and uploaded via bluetooth to a database for review. They will continue to receive routine obstetric and diabetes care.

Detailed Description

This is a randomized controlled trial of postprandial ambulation to decrease birthweight percentile in patients with gestational diabetes.

Patients who are diagnosed with gestational diabetes. and enrolled in the Diabetes in Pregnancy Program in the Division of Maternal Fetal Medicine at Women and Infants Hospital of Rhode Island will be approach for inclusion in the study. After consent is obtained, patients with gestational diabetes. will be randomized into one of two groups.

  • Group 1: intervention group: 20 minutes of walking after meals
  • Group 2: non-intervention group: routine activity

Randomization will occur via computer generated randomization in blocks of 10. After consent is obtained the participants will be randomized via REDCap. They will then receive counseling specific to their group. They will be provided with an activity monitor and instructed on how to use as well as charge and upload data. They will be provided with the information from the manufacturer as well as trouble shooting guide.

As is the standard of care in this clinic, both groups would be equipped with glucometers and diabetic testing supplies. Both groups would receive the same diabetes and nutrition counseling from qualified nursing staff. Additionally, all participants will be provided with Bluetooth enabled pedometers. Those participants assigned to the intervention group would be instructed to walk for 20 minutes within the first two hours following each meal, while those assigned to the routine activity group will receive standard exercise counseling per American College of Obstetricians and Gynecologists and the American Diabetes Association.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to 50 Years (Adult)
Sex
Female
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Patients who are diagnosed with gestational diabetes and receive care at the Maternal Fetal Medicine Diabetes in Pregnancy Program and who are fluent in English or Spanish.

Exclusion Criteria

  • •Pre-existing type 1 or type 2 diabetes, and those diagnosed with gestational diabetes in the first trimester. Patients who are either physically unable to ambulate or who have other contraindications to ambulation.

Arms & Interventions

Postprandial Ambulation

Experimental

Participants are counseled to walk for 20 minutes within 2 hours following meals daily.

Intervention: Postprandial ambulation (Behavioral)

Routine exercise counseling

No Intervention

Participants are counseled on routine ADA recommendations for 30 minutes of low-impact exercise 5 times a week

Outcomes

Primary Outcomes

Infant birthweight percentile

Time Frame: Single time point - at birth

Birthweight percentile for gestational age for neonatal sex

Secondary Outcomes

  • fetal macrosomia(Single time point - at birth)
  • neonatal hypoglycemia treatment(within 48 hours of birth)
  • need for insulin or metformin during pregnancy(from diagnosis to delivery of infant)
  • infant birthweight(Single time point - at birth)
  • mode of delivery(Single time point)

Investigators

Sponsor
Women and Infants Hospital of Rhode Island
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Anna Whelan

Clinical and Research Fellow, Principal Investigator

Women and Infants Hospital of Rhode Island

Study Sites (1)

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