CClinicalTrials.gg
CompletedNCT04193072Updated Sep 29, 2023

Imagery Ability in Obstetric Brachial Plexus Palsy

An observational study in Brachial Plexus Palsy and Image, Body, sponsored by Istanbul Medipol University Hospital. Completed at 1 site in Turkey. Open to participants aged 8 Years to 18 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2023-09-29.

Sponsored by Istanbul Medipol University Hospital · Observational

Study type
Observational
Model
Case-control
Time perspective
Prospective
Enrollment
40
Ages
8 Years to 18 Years
Sex
All
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Study summary

Obstetric brachial plexus palsy (OBPP) is the paralysis of the ipsilateral upper extremity after a brachial plexus injury that occurs during labor. Imagery is to rehearse sensorial experiences in the mind such as auditory, visual, tactile, olfactory, gustatory or kinesthetic sensation. Imagery is used as a new technique in rehabilitation recently. Various studies have reported the importance of imagery and using imagery as a rehabilitation technique in different neurologic and orthopedic conditions. This study aimed to evaluate imagery ability in children with OBPP.

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Conditions studied

  • Brachial Plexus Palsy
  • Image, Body

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Keywords

  • brachial plexus
  • imagery
  • body image
  • sensation
  • questionnaires
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In context

Paralysis

750 studies on the registry are indexed under Paralysis; 133 are open to participants now.

This study's enrollment of 40 is below the median of 60 across 199 observational studies indexed under Paralysis.

Browse Paralysis studies →

Lead sponsor

Istanbul Medipol University Hospital is the lead sponsor of 350 studies on the registry; 58 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
8 Years to 18 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Children with obstetric brachial plexus palsy and healthy children.

Inclusion criteria

  • Ages between 8-18 years
  • Children with OBPP Narakas's classification system rating of Type 1, Type 2a, Type 2b, or Type 3
  • Standardized mini-mental state examination score >24
  • With no physical or neurological condition affecting motor development

Exclusion criteria

Exclusion Criteria:

  • Narakas's classification system rating of Type 4
  • Standardized mini-mental state examination score \<24
  • Surgical operation in last 6 months
  • Physical or neurological conditions
  • Refuse to attend to the study
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Study design

Observational model
Case-control
Time perspective
Prospective
Enrollment
40 participants (actual)
Patient registry
No

Groups and cohorts

  • Obstetric brachial plexus palsy

    Behavioral: Assessment of imagery ability

  • Healthy

    Behavioral: Assessment of imagery ability

Interventions

  • BehavioralAssessment of imagery ability

    Movement imagery, kinesthetic imagery, and visual imagery ability assessed.

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What researchers measure

Primary outcomes

  1. Movement Imagery Questionnaire-3

    Movement Imagery Questionnaire-3 is a 12-item questionnaire to assess an individual's ability to achieve specific four movements using internal visual imagery, external visual imagery, and kinesthetic imagery.

    Time frame: 2 weeks

  2. Kinesthetic and Visual Imagery Questionnaire-20

    Kinesthetic and Visual Imagery Questionnaire-20 assess an individual's ability to visualize and feel imagined movements.

    Time frame: 2 weeks

  3. Active Movement Scale

    Active Movement Scale evaluates 15 joint movements in the upper extremity against gravity and gravity-eliminated positions. Each movement is given a score between 0-7: 0 means no contraction, 7 means full range of motion.

    Time frame: 1 week

  4. Narakas's Sensory Grading System

    Narakas's Sensory Grading System evaluates the response to painful stimuli in the upper extremity with 0-3-point scale: 0 indicates no reaction, 3 indicates a normal reaction.

    Time frame: 1 week

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Study locations

1 site
  • Istanbul Medipol University Hospital
    Istanbul, Turkey
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References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 29, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT04193072
Lead sponsor
Istanbul Medipol University Hospital
Responsible party
Nursena Şengün (Physiotherapist, Istanbul Medipol University Hospital) — Principal investigator
First posted
Dec 10, 2019
Start date
Oct 2, 2017
Primary completion
Jan 27, 2018
Completion
Mar 25, 2018
Last update
Sep 29, 2023

Study contacts

Nursena Şengün, PT, MSc
principal investigator · Medipol University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Sep 2023. You cannot join it, but the record below documents what was studied.

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