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Acute Effects of Motor Imagery Exercises in Individuals With Pregnancy-Related Lumbopelvic Pain

Acute Effects of Motor Imagery Exercises in Individuals With Pregnancy-Related Lumbopelvic Pain

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07516743
Enrollment
40
Registered
2026-04-08
Start date
2026-04-01
Completion date
2026-07-13
Last updated
2026-07-14

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

Conditions

Pregnancy-related Lumbopelvic Pain

Brief summary

The aim of this study is to investigate the effects of single-session motor imagery exercises on pain and motor imagery in individuals with pregnancy-related lumbopelvic pain.

Interventions

A single session of motor imagery exercise will be performed according to the PETTLEP model.

OTHERPlacebo Motor Imagery Exercise

A single session of placebo motor imagery exercise will be performed according to the PETTLEP model.

Sponsors

KTO Karatay University
Lead SponsorOTHER

Study design

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

Eligibility

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

Inclusion criteria

* Be in a singleton, uncomplicated pregnancy. * Lumbopelvic pain (lower back or pelvic girdle pain) must have begun during pregnancy. * Be between the 12th and 40th weeks of pregnancy. * Be capable of understanding motor imagery training and following instructions.

Exclusion criteria

* A history of chronic lower back pain present before pregnancy and persisting during pregnancy. * Symptoms of neuropathic lower back pain (e.g., radiculopathy), inflammatory conditions such as tumors, infections, compression fractures, or ankylosing spondylitis that are specific causes of lower back or pelvic pain, a history of previous spinal or pelvic surgery, * Severe neurological disorders, metabolic disorders, or severe orthopedic conditions, * Medical restrictions that prevent exercise or maintaining certain positions (e.g., lying on the back).

Design outcomes

Primary

MeasureTime frameDescription
Pain SeverityBaseline and immediately post-interventionThe pain of the participants will be evaluated with a 10 cm Visual Analog Scale before the treatment and at the end of the application. "0" means no pain, "10" means excruciating pain. Results will be recorded in cm.
Motor ImageryBaseline and immediately post-interventionMotor imagery ability will be assessed using the Movement Imagery Questionnaire (MIQ). The questionnaire consists of items assessing visual imagery (clarity of the image) and kinesthetic imagery (intensity of the sensation). Each item is scored on a 7-point scale (1 = very hard to imagine, 7 = very easy to imagine). Subscale scores (visual and kinesthetic) and a total score will be calculated. Higher scores indicate better motor imagery ability.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 15, 2026