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Motor Imagery in High-Risk Pregnants

NCT05946252 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 76

Last updated 2024-01-31

No results posted yet for this study

Summary

The aim of this study is to determine the acute effects of motor imagery exercises on fetal heart rate, uterine contractions, maternal heart rate, blood pressure, oxygen saturation and well-being in high-risk pregnant women.

Conditions

  • Pregnancy, High Risk

Interventions

OTHER

Motor imagery

Motor imagery will be performed according to the PETTLEP (Physical,Environment,Task,Time,Learn,Emotion,Perspective) model for 15 minutes. 1. To imagine walking activity in different environments (seaside, beach, walking path). 2. The rest activity will be imagined by sitting on a bench. 3. Upper extremity strengthening exercises with dumbbells, lower extremity strengthening exercises with elastic band and trunk-oriented bridging, posterior pelvic tilt and table top stabilization exercises will be visualized. 4. The rest activity will be imagined by sitting on a bench. 5. Imagination will end with homecoming and domestic activities.

OTHER

Diaphragmatic breathing

Diaphragmatic breathing will be shown to pregnant women in the supine position, eyes closed, with one hand on the chest and the other hand on the abdomen. This practice will last for five minutes.

Sponsors & Collaborators

  • Izmir University of Economics

    lead OTHER

Principal Investigators

  • Seda Yakıt Yeşilyurt, PT, PhD · Izmir University of Economics

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
45 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-08-01
Primary Completion
2023-10-02
Completion
2024-01-05

Countries

  • Turkey (Türkiye)

Study Locations

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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 NCT05946252 on ClinicalTrials.gov