NCT02451644

Brief Summary

The study examines the association between the amount of physical activity of the patient, ie the number of steps daily / weekly, and the pregnancy rate after embryo transfer.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
200

participants targeted

Target at P50-P75 for not_applicable pregnancy

Timeline
Completed

Started Jun 2015

Longer than P75 for not_applicable pregnancy

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

May 9, 2015

Completed
13 days until next milestone

First Posted

Study publicly available on registry

May 22, 2015

Completed
10 days until next milestone

Study Start

First participant enrolled

June 1, 2015

Completed
4.1 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 1, 2019

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

July 1, 2019

Completed
Last Updated

April 24, 2018

Status Verified

April 1, 2018

Enrollment Period

4.1 years

First QC Date

May 9, 2015

Last Update Submit

April 21, 2018

Conditions

Pregnancy

Outcome Measures

Primary Outcomes (1)

  • Physical activity as assessed by number of steps recorded by pedometer

    4 weeks

Study Arms (1)

high risk for PTD with pedometer

EXPERIMENTAL

Patient with high risk for preterm delivery including short cervix or rapture of membranes

Device: pedometer

Interventions

pedometerDEVICE

patient will cary pedometer

high risk for PTD with pedometer

Eligibility Criteria

Age18 Years - 45 Years
Sexmale
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • Participant speaks Hebrew or English speakers
  • The participant is eligible to legally provide informed consent

You may not qualify if:

  • The Subject in the wheelchair-bound or limited walking
  • Participant refuses to give informed consent

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Shalom Mazaki tovi

Ramat Gan, Israel

RECRUITING

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
PREVENTION
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER GOV
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Director of high risk Department

Study Record Dates

First Submitted

May 9, 2015

First Posted

May 22, 2015

Study Start

June 1, 2015

Primary Completion

July 1, 2019

Study Completion

July 1, 2019

Last Updated

April 24, 2018

Record last verified: 2018-04

Locations

IL(1)