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Mindfetalness to Improve Pregnancy Outcome

NCT02865759 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 39000

Last updated 2020-07-21

No results posted yet for this study

Summary

To improve pregnancy outcome, 39 000 pregnant women will be randomized to receive information about Mindfetalness or to routine care. The level of randomization will be the antenatal clinics in the Stockholm area.

Conditions

  • Pregnancy Outcomes

Interventions

BEHAVIORAL

Mindfetalness

The pregnant woman is motivated to practice Mindfetalness verbally, by a brochure and at a website.

Sponsors & Collaborators

  • Karolinska Institutet

    collaborator OTHER

  • Göteborg University

    collaborator OTHER

  • Sophiahemmet University

    lead OTHER

Principal Investigators

  • Ingela Rådestad, PhD · Sophiahemmet University

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
SINGLE
Model
PARALLEL

Eligibility

Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-11-01
Primary Completion
2018-06-30
Completion
2018-06-30

Countries

  • Sweden

Study Locations

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Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02865759 on ClinicalTrials.gov