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NCT05093842 · ClinicalTrials.gov registry record · NA
Sedentary Behavior Reduction in Pregnancy Intervention Study
A NA study of Sedentary Behavior and Pregnancy Complications, sponsored by University of Pittsburgh.
- Completed
- Registry status
- NA
- Development phase
- 51
- Enrollment target
- 1
- Study location
NCT05093842 is a NA study of Sedentary Behavior and Pregnancy Complications that has completed, run by University of Pittsburgh. The registered enrollment target is 51 participants, below the 756-participant average among 42 other Sedentary Behavior trials with a reported enrollment target (93% lower). The trial reports 1 study location across 1 state.
The verdict
NCT05093842, a NA study of Sedentary Behavior and Pregnancy Complications, has completed, sponsored by University of Pittsburgh.
- COMPLETED
- Registry status
- NA
- Development phase
- 51 participants
- Enrollment target
- 1
- Study location
Study Summary
This pilot and feasibility study will enroll newly pregnant women at risk for high sedentary behavior (SED) and elevated APO risk (n=53) and will randomize them to either a SED reduction intervention or control. Research aims include to: 1) demonstrate our ability to decrease SED and increase standing and light activity in pregnant women; 2) evaluate feasibility; and 3) gather preliminary effects on clinical outcomes including APOs, cardiometabolic risk factors, well-being, and fetal outcomes.
Conditions Studied
Interventions
- BEHAVIORAL Sedentary Behavior Reduction
- BEHAVIORAL Information on Physical Activity Recommendations during Pregnancy
Study Locations (1)
Pennsylvania
- University of Pittsburgh, Department of Health and Human Development, 32 Oak Hill Court, Room 220 - Pittsburgh
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 51 participants |
| Start Date | 2021-10-04 |
| Est. Completion | 2023-06-30 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05093842
The ClinicalTrials.gov registry entry for NCT05093842 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 51 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 756-participant average among 42 other Sedentary Behavior trials with a reported enrollment target (93% lower). The listed sponsor is University of Pittsburgh, which has 1,238 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Sedentary Behavior appearing as the primary indexed condition, and to 2 interventions - of which Sedentary Behavior Reduction is the first listed.
NCT05093842 reports 1 study location spanning 1 distinct geographic area - top geographies include Pennsylvania.
Frequently Asked Questions
What is clinical trial NCT05093842 about?
NCT05093842 is a clinical study titled "Sedentary Behavior Reduction in Pregnancy Intervention Study". This pilot and feasibility study will enroll newly pregnant women at risk for high sedentary behavior (SED) and elevated APO risk (n=53) and will randomize them to either a SED reduction intervention or control. Research aims include to: 1) demonstrate our ability to decrease SED and increase standi...
What is the current status of trial NCT05093842?
This trial is currently completed. It is a NA study. The enrollment target is 51 participants. The study started on 2021-10-04. Estimated completion is 2023-06-30.
What conditions does trial NCT05093842 study?
This clinical trial studies the following conditions: Sedentary Behavior, Pregnancy Complications.
What interventions are being tested in trial NCT05093842?
The interventions under investigation include: Sedentary Behavior Reduction (BEHAVIORAL), Information on Physical Activity Recommendations during Pregnancy (BEHAVIORAL).
Who is sponsoring clinical trial NCT05093842?
This trial is sponsored by University of Pittsburgh, which has 1,238 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT05093842 being conducted?
This trial has 1 study location across Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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