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Motor Imagery in High-Risk Pregnants

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05946252
Enrollment
76
Registered
2023-07-14
Start date
2023-08-01
Completion date
2024-01-05
Last updated
2024-01-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pregnancy, High Risk

Brief 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.

Detailed description

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.

Interventions

OTHERMotor 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.

OTHERDiaphragmatic 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

Izmir University of Economics
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Intervention model description

This is a prospective randomized controlled study.

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 45 Years
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
Maternal self well-beingat baselineWell-being will be assessed on a numbered classification scale-11. '0' indicates worse self well-being, '10' indicates excellent self well-being.

Secondary

MeasureTime frameDescription
Maternal heart rateat baselineHeart rate measurements will be made with an arm type digital sphygmomanometer.
Maternal blood pressure (systolic pressure)at baselineBlood pressure measurements will be made with an arm type digital sphygmomanometer. Systolic blood pressure and diastolic blood pressure will be assessed.
Maternal blood pressure (diastolic pressure)at baselineBlood pressure measurements will be made with an arm type digital sphygmomanometer. Systolic blood pressure and diastolic blood pressure will be assessed.
Maternal self well-beingimmediately after interventionWell-being will be assessed on a numbered classification scale-11. '0' indicates worse self well-being, '10' indicates excellent self well-being.
Fetal Heart Rateat baselineFetal heart rate will be monitored with a cardiotachometer (Philips Avalon Fetal Monitor).
Uterine contractions severityat baselineUterine contractions severity will be monitored with a cardiotachometer (Philips Avalon Fetal Monitor).
oxygen saturationat baselineFinger type pulse oximeter will be attached and peripheral oxygen saturation will be monitored.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026