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Completed

NCT Number: NCT05946252

Motor Imagery in High-Risk Pregnants

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.

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Key information

Age range

18 year–45 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Health Sciences University İzmir Tepecik Education and Research Hospital Gynecology and Obstetrics Clinic

Izmir, Turkey (Türkiye)

About this study

Bed rest is often recommended in high-risk pregnant women to prevent complications from reaching dangerous levels.

Pregnant women recommended bed rest can benefit from exercise in order to overcome this process more easily, to reduce the negative consequences of inactivity and to prevent possible risks.

However, there may be differences between the view of high-risk pregnant women and the view of healthy pregnant women. Motor imagery refers to a mental process in which an individual mentally imagines that movement without actually eliciting an active movement. Studies have shown that similar brain regions are activated during movement performance and movement imagery. It has been reported in the literature that progressive relaxation exercises performed under mental/motor imagery guidance in healthy pregnant women and pregnant women lead to an improvement in maternal anxiety, stress and fetal attachment scales and a decrease in maternal systolic/diastolic blood pressure. However, as far as the investigators know, there is no study that applies the exercise protocol that can be given to healthy pregnant women to high-risk pregnant women with motor imagery and examines acute responses on fetal and maternal parameters.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Risky pregnant women who have completed the 12th week of pregnancy, received inpatient treatment and have any of the following risk factors will be included in the study:

  • Pregnant women who are at risk for obstetric outcomes such as cervical insufficiency, multiple pregnancy and uncontrolled gestational diabetes, and physical activity restriction is recommended due to these conditions, and exercise is contraindicated,
  • Pregnant women with a maternal body mass index above 30, which causes them to be physically inactive

Exclusion criteria

  • Pregnant women who are at risk for obstetric outcomes such as gestational diabetes mellitus and pregnancy-induced hypertension, but physical activity is recommended
  • Pregnant women with severe cardiovascular, pulmonary and systemic disorders
  • Pregnant women with psychological seizure disorders
  • Pregnant women who do not have any mental problems that prevent cooperation and understanding
  • Pregnant women with any medical condition that prevents the safe and effective implementation of interventions.
  • Pregnant women in other high-risk groups (such as early membrane rupture, placenta previa, preeclampsia) that may have early intervention in terms of obstetric outcomes.

Treatment and study plan

motor imagery

Other

Motor imagery will be performed according to the PETTLEP (Physical,Environment,Task,Time,Learn,Emotion,Perspective) model for 15 minutes.

  • To imagine walking activity in different environments (seaside, beach, walking path).
  • The rest activity will be imagined by sitting on a bench.
  • 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.
  • The rest activity will be imagined by sitting on a bench.
  • Imagination will end with homecoming and domestic activities.

Diaphragmatic breathing

Other

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.

Primary outcomes

  1. Maternal self well-being

    Time frame: at baseline

    Well-being will be assessed on a numbered classification scale-11. '0' indicates worse self well-being, '10' indicates excellent self well-being.

Secondary outcomes

  1. Maternal self well-being

    Time frame: immediately after intervention

    Well-being will be assessed on a numbered classification scale-11. '0' indicates worse self well-being, '10' indicates excellent self well-being.

  2. Maternal heart rate

    Time frame: at baseline

    Heart rate measurements will be made with an arm type digital sphygmomanometer.

  3. Maternal heart rate

    Time frame: in the 7th minutes of the intervention

    Heart rate measurements will be made with an arm type digital sphygmomanometer.

  4. Maternal heart rate

    Time frame: immediately after intervention

    Heart rate measurements will be made with an arm type digital sphygmomanometer.

  5. Maternal blood pressure (systolic pressure)

    Time frame: at baseline

    Blood pressure measurements will be made with an arm type digital sphygmomanometer.

    Systolic blood pressure and diastolic blood pressure will be assessed.

  6. Maternal blood pressure (systolic pressure)

    Time frame: in the 7th minutes of the intervention

    Blood pressure measurements will be made with an arm type digital sphygmomanometer.

    Systolic blood pressure and diastolic blood pressure will be assessed.

  7. Maternal blood pressure (systolic pressure)

    Time frame: immediately after intervention

    Blood pressure measurements will be made with an arm type digital sphygmomanometer.

    Systolic blood pressure and diastolic blood pressure will be assessed.

  8. Maternal blood pressure (diastolic pressure)

    Time frame: at baseline

    Blood pressure measurements will be made with an arm type digital sphygmomanometer.

    Systolic blood pressure and diastolic blood pressure will be assessed.

  9. Maternal blood pressure (diastolic pressure)

    Time frame: in the 7th minutes of the intervention

    Blood pressure measurements will be made with an arm type digital sphygmomanometer.

    Systolic blood pressure and diastolic blood pressure will be assessed.

  10. Maternal blood pressure (diastolic pressure)

    Time frame: immediately after intervention

    Blood pressure measurements will be made with an arm type digital sphygmomanometer.

    Systolic blood pressure and diastolic blood pressure will be assessed.

  11. oxygen saturation

    Time frame: at baseline

    Finger type pulse oximeter will be attached and peripheral oxygen saturation will be monitored.

  12. oxygen saturation

    Time frame: in the 7th minutes of the intervention

    Finger type pulse oximeter will be attached and peripheral oxygen saturation will be monitored.

  13. oxygen saturation

    Time frame: immediately after intervention

    Finger type pulse oximeter will be attached and peripheral oxygen saturation will be monitored.

  14. Fetal Heart Rate

    Time frame: at baseline

    Fetal heart rate will be monitored with a cardiotachometer (Philips Avalon Fetal Monitor).

  15. Fetal Heart Rate

    Time frame: in the 7th minutes of the intervention

    Fetal heart rate will be monitored with a cardiotachometer (Philips Avalon Fetal Monitor).

  16. Fetal Heart Rate

    Time frame: immediately after intervention

    Fetal heart rate will be monitored with a cardiotachometer (Philips Avalon Fetal Monitor).

  17. Uterine contractions severity

    Time frame: at baseline

    Uterine contractions severity will be monitored with a cardiotachometer (Philips Avalon Fetal Monitor).

  18. Uterine contractions severity

    Time frame: in the 7th minutes of the intervention

    Uterine contractions severity will be monitored with a cardiotachometer (Philips Avalon Fetal Monitor).

  19. Uterine contractions severity

    Time frame: immediately after intervention

    Uterine contractions severity will be monitored with a cardiotachometer (Philips Avalon Fetal Monitor).

Sponsors and collaborators

Lead sponsor

Izmir University of Economics

Other

Registry information

Official study title

Acute Effect of Motor Imagery in High-Risk Pregnants: A Randomized Controlled Pilot Study

Important dates

Study start
2023
Primary completion
2023
Study completion
2024
First posted
Jul 14, 2023
Registry last updated
Jan 31, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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