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Anchoring and Postural Stability

17 september 2026 bijgewerkt door: William J. Hanney, University of Central Florida

Anchoring and Its Effects on Postural Stability

This study will compare standing balance in adults ages 18 to 50 during normal standing, inward anchoring, and outward anchoring. Anchoring involves standing with the feet wider than shoulder width and trying to pull the legs together or push them apart without moving the feet. Participants will complete all three conditions in a randomly assigned order. A researcher will use a handheld force-measuring instrument at six points on the pelvis to measure how much pressure participants can resist before a foot lifts from the floor. Participants will also rate how stable they feel after each anchoring condition. The first 18 participants will repeat assessments to evaluate measurement consistency. Participation is expected to last 60 minutes, or 90 minutes for those completing repeat assessments.

Studie Overzicht

Gedetailleerde beschrijving

The study will enroll 72 adults from the University of Central Florida community. Participants will be randomized with equal probability to one of six counterbalanced orders of normal stance, inward anchoring, and outward anchoring. Every participant will complete all three conditions.

Inward anchoring involves attempting to draw the legs toward one another without moving the feet. Outward anchoring involves attempting to press the legs away from one another without moving the feet. Both anchoring conditions use a stance wider than shoulder width. Participants will wear their usual athletic footwear.

The same tester will apply a microFET2 handheld dynamometer at the right and left anterior superior iliac spines, iliac crests, and posterior superior iliac spines. Applied pressure will increase until the sole of the foot closest to the tester leaves the floor, at which point force will be recorded in newtons. Each site will be tested three times in each stance. Rest periods will be one minute between sets within a stance and two minutes between stances. Instructions for the next stance will be given during the final minute of the between-stance rest period.

After each anchoring condition, participants will rate perceived stability. The first 18 participants will complete additional repeat assessments for intrarater reliability analysis. The protocol plans repeated-measures analyses for stance/order comparisons and intraclass correlation coefficients for reliability.

Studietype

Ingrijpend

Inschrijving (Geschat)

72

Fase

  • Niet toepasbaar

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studiecontact

Studie Locaties

    • Florida
      • Orlando, Florida, Verenigde Staten, 32816
        • Werving
        • University of Central Florida Spine and Mobility Lab
        • Contact:

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

18 jaar tot 50 jaar (Volwassen)

Accepteert gezonde vrijwilligers

Ja

Geslachten die in aanmerking komen voor studie

Allemaal

Beschrijving

Inclusion Criteria:

  • Adults aged 18-50 years.
  • Able to provide informed consent and independently read, write, and communicate in English.

Exclusion Criteria:

  • History of neurological or vestibular conditions affecting balance, such as stroke, Parkinson's disease, multiple sclerosis, or vertigo, or uncorrected/inadequately corrected visual deficits affecting postural control.
  • Lower-extremity or spinal injury, orthopedic surgery, or a musculoskeletal condition within the past 6-12 months that may affect balance, force production, or safe participation.
  • Current pain or dysfunction limiting safe standing or weight-bearing tasks.
  • Use of medications that may affect balance, coordination, or muscle performance, such as muscle relaxants, opioids, or sedatives.
  • A cardiovascular or systemic condition that makes participation unsafe, such as uncontrolled hypertension, dizziness, or syncope, or inability to stand independently for the duration of testing.

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

  • Primair doel: Screening
  • Toewijzing: Gerandomiseerd
  • Interventioneel model: Crossover-opdracht
  • Masker: Dubbele

Wapens en interventies

Deelnemersgroep / Arm
Interventie / Behandeling
Experimenteel: Normal Stance → Inward Anchoring → Outward Anchoring

Participants complete normal stance, then inward anchoring, then outward anchoring. The same force assessments are performed in each condition, with two minutes of rest between conditions.

Participants stand normally while the tester performs the protocol's pelvic force assessments. This condition provides the within-participant comparison for the two anchoring techniques

Participants stand upright with their feet wider than shoulder width and attempt to pull their legs toward each other without moving the feet. They maintain the position during the pelvic force assessments.

Participants stand upright with their feet wider than shoulder width and attempt to push their legs away from each other without moving the feet. They maintain the position during the pelvic force assessments.

Experimenteel: Normal Stance → Outward Anchoring → Inward Anchoring

Participants complete normal stance, then outward anchoring, then inward anchoring. The same force assessments are performed in each condition, with two minutes of rest between conditions.

Participants stand normally while the tester performs the protocol's pelvic force assessments. This condition provides the within-participant comparison for the two anchoring techniques

Participants stand upright with their feet wider than shoulder width and attempt to pull their legs toward each other without moving the feet. They maintain the position during the pelvic force assessments.

Participants stand upright with their feet wider than shoulder width and attempt to push their legs away from each other without moving the feet. They maintain the position during the pelvic force assessments.

Experimenteel: Outward Anchoring → Normal Stance → Inward Anchoring

Participants complete outward anchoring, then normal stance, then inward anchoring. The same force assessments are performed in each condition, with two minutes of rest between conditions.

Participants stand normally while the tester performs the protocol's pelvic force assessments. This condition provides the within-participant comparison for the two anchoring techniques

Participants stand upright with their feet wider than shoulder width and attempt to pull their legs toward each other without moving the feet. They maintain the position during the pelvic force assessments.

Participants stand upright with their feet wider than shoulder width and attempt to push their legs away from each other without moving the feet. They maintain the position during the pelvic force assessments.

Experimenteel: Outward Anchoring → Inward Anchoring → Normal Stance

Participants complete outward anchoring, then inward anchoring, then normal stance. The same force assessments are performed in each condition, with two minutes of rest between conditions.

Participants stand normally while the tester performs the protocol's pelvic force assessments. This condition provides the within-participant comparison for the two anchoring techniques

Participants stand upright with their feet wider than shoulder width and attempt to pull their legs toward each other without moving the feet. They maintain the position during the pelvic force assessments.

Participants stand upright with their feet wider than shoulder width and attempt to push their legs away from each other without moving the feet. They maintain the position during the pelvic force assessments.

Experimenteel: Inward Anchoring → Normal Stance → Outward Anchoring

Participants complete inward anchoring, then normal stance, then outward anchoring. The same force assessments are performed in each condition, with two minutes of rest between conditions.

Participants stand normally while the tester performs the protocol's pelvic force assessments. This condition provides the within-participant comparison for the two anchoring techniques

Participants stand upright with their feet wider than shoulder width and attempt to pull their legs toward each other without moving the feet. They maintain the position during the pelvic force assessments.

Participants stand upright with their feet wider than shoulder width and attempt to push their legs away from each other without moving the feet. They maintain the position during the pelvic force assessments.

Experimenteel: Inward Anchoring → Outward Anchoring → Normal Stance

Participants complete inward anchoring, then outward anchoring, then normal stance. The same force assessments are performed in each condition, with two minutes of rest between conditions.

Participants stand normally while the tester performs the protocol's pelvic force assessments. This condition provides the within-participant comparison for the two anchoring techniques

Participants stand upright with their feet wider than shoulder width and attempt to pull their legs toward each other without moving the feet. They maintain the position during the pelvic force assessments.

Participants stand upright with their feet wider than shoulder width and attempt to push their legs away from each other without moving the feet. They maintain the position during the pelvic force assessments.

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Mean Break-Point Force at the Right Anterior Superior Iliac Spine
Tijdsspanne: Day 1

A microFET2 handheld dynamometer is applied at the right anterior superior iliac spine during normal stance, inward anchoring, and outward anchoring. Force in newtons is recorded when the sole of the foot closest to the tester leaves the floor. Three readings are collected per stance

Day 1
Mean Break-Point Force at the Left Anterior Superior Iliac Spine
Tijdsspanne: Day 1

A microFET2 handheld dynamometer is applied at the left anterior superior iliac spine during normal stance, inward anchoring, and outward anchoring. Force in newtons is recorded when the sole of the foot closest to the tester leaves the floor. Three readings are collected per stance.

Day 1
Mean Break-Point Force at the Right Iliac Crest
Tijdsspanne: Day 1

A microFET2 handheld dynamometer is applied at the right iliac crest during normal stance, inward anchoring, and outward anchoring. Force in newtons is recorded when the sole of the foot closest to the tester leaves the floor. Three readings are collected per stance

Day 1
Mean Break-Point Force at the Left Iliac Crest
Tijdsspanne: Day 1

A microFET2 handheld dynamometer is applied at the left iliac crest during normal stance, inward anchoring, and outward anchoring. Force in newtons is recorded when the sole of the foot closest to the tester leaves the floor. Three readings are collected per stance.

Day 1
Mean Break-Point Force at the Right Posterior Superior Iliac Spine
Tijdsspanne: Day 1

A microFET2 handheld dynamometer is applied at the right posterior superior iliac spine during normal stance, inward anchoring, and outward anchoring. Force in newtons is recorded when the sole of the foot closest to the tester leaves the floor. Three readings are collected per stance.

Day 1
Mean Break-Point Force at the Left Posterior Superior Iliac Spine
Tijdsspanne: Day 1

A microFET2 handheld dynamometer is applied at the left posterior superior iliac spine during normal stance, inward anchoring, and outward anchoring. Force in newtons is recorded when the sole of the foot closest to the tester leaves the floor. Three readings are collected per stance.

Day 1
Perceived Stability Rating After Inward Anchoring
Tijdsspanne: Day 1

After inward anchoring, participants answer how stable they felt during that stance. Ratings range from 0 (not at all stable) to 10 (completely stable); 5 means neutral, or the same stability as normal standing. Higher scores indicate greater perceived stability.

Day 1
Perceived Stability Rating After Outward Anchoring
Tijdsspanne: Day 1

After outward anchoring, participants answer how stable they felt during that stance. Ratings range from 0 (not at all stable) to 10 (completely stable); 5 means neutral, or the same stability as normal standing. Higher scores indicate greater perceived stability

Day 1

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Onderzoekers

  • Hoofdonderzoeker: William J Hanney, PhD, University of Central Florida

Publicaties en nuttige links

De persoon die verantwoordelijk is voor het invoeren van informatie over het onderzoek stelt deze publicaties vrijwillig ter beschikking. Dit kan gaan over alles wat met het onderzoek te maken heeft.

Algemene publicaties

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start (Werkelijk)

23 augustus 2026

Primaire voltooiing (Geschat)

30 september 2027

Studie voltooiing (Geschat)

2 mei 2028

Studieregistratiedata

Eerst ingediend

9 september 2026

Eerst ingediend dat voldeed aan de QC-criteria

17 september 2026

Eerst geplaatst (Werkelijk)

24 september 2026

Updates van studierecords

Laatste update geplaatst (Werkelijk)

24 september 2026

Laatste update ingediend die voldeed aan QC-criteria

17 september 2026

Laatst geverifieerd

1 september 2026

Meer informatie

Termen gerelateerd aan deze studie

Plan Individuele Deelnemersgegevens (IPD)

Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?

NEE

Informatie over medicijnen en apparaten, studiedocumenten

Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel

Nee

Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct

Nee

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