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Fit for Two: Incorporating Wearable Trackers Into Clinical Care for Pregnant Women With Diabetes (FFT)

Not Applicable
Completed
Conditions
Physical Activity
Type 2 Diabetes Mellitus
Interventions
Behavioral: physical activity counseling & Fitbit
Registration Number
NCT03302377
Lead Sponsor
University of California, San Diego
Brief Summary

This study will investigate the feasibility of an intervention to increase physical activity in pregnant women with diabetes by incorporating a brief in-person counseling session and Fitbit activity trackers into routine clinical care

Detailed Description

This is a small, one-armed pilot study testing a physical activity intervention for pregnant patients with diabetes. The intervention will use both counseling and technology (a FitBit physical activity tracker and smartphone app) to create an individualized, interactive program for each patient. The primary aims of the study are to assess the feasibility of recruiting patients and implementing the program in the clinical setting, and the acceptability of the program for patients and clinicians. Participants will receive a counseling session based on the principles of motivational interviewing to help them set physical activity and step goals, then the interventionist will help them personalize the Fitbit app to their goals. Participants are instructed to continue adaptive goal setting and email their goals and activity weekly to their physicians. In addition to assessing feasibility and acceptability, we will also evaluate change in activity to explore potential efficacy.

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
19
Inclusion Criteria
  • diagnosed with type 2 diabetes or gestational diabetes
  • currently pregnant
  • in week 5-25 of gestation
  • under active (<100 minutes/week of physical activity)
  • access to a smartphone
Exclusion Criteria
  • any medical condition that would make unsupervised activity unsafe or unfeasible, as determined by their physician
  • moving from the area within 3 months

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Physical activity interventionphysical activity counseling & FitbitParticipants will receive an individual counseling session in the clinic to help them set physical activity and step goals. They will then receive a Fitbit wrist monitor and help personalizing the Fitbit app. They will send weekly emails to their physicians reporting their goals and current activity. They will return at 12 weeks to engage in a semi-structured interview to give their overall impressions of the intervention.
Primary Outcome Measures
NameTimeMethod
Acceptability12 weeks

Determined by participant feedback (% indicating satisfaction with intervention)

Feasibility of recruitmentbaseline

Determined by percent of those screened who enroll in the study

Retention12 weeks

Determined by retention (%)

Secondary Outcome Measures
NameTimeMethod
Physical activity change12 weeks

Change in objectively measured physical activity from baseline to follow-up as measured by hip-worn ActiGraph GT3X+ accelerometers, adjusting for baseline

Trial Locations

Locations (1)

University of California, San Diego

🇺🇸

La Jolla, California, United States

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