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Healthy VolunteersNCT03032393

The Effect of Power Posing on Timed Up and Go Test Score

A study testing high-power and low-power in people with Healthy Volunteers, run by Youngstown State University at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

This study determines the effects of posture on time up and go test. Half of the subjects will assume a high-power posture, while the other half will assume a low-power posture. Read more about this study

Who is it for?
Ages 18 to 65 yearsHealthy volunteers can take part
Conditions the study is for
Healthy Volunteers
What is being tested?
high-power and low-power
Could I receive a placebo?
No, everyone receives an active treatment
How many people
30 participants
Where
1 siteUnited States
Study dates
3 Feb 2017to 31 Dec 2017
Phase
Interventional
Are there results?
Yes, posted in the registrySummary in the doctors' view

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 65 years
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • male or female, age 18 to 65, with all 4 extremities intact, and ability to stand still for 20 seconds.

Who cannot join

  • unable to stand with their feet together or one foot apart for at least 20 seconds, unable to wrap their arms around their torso or keep their hands on their hips for 20 seconds, unable to perform sit to stand transfer and ambulation independently, and cognitive impairments that interfere with the experimental procedures.

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Youngstown State University

    Youngstown, Ohio, 44555

Other trials in United States

About this study

Official title: The Effects of Posture on Timed up and go

This study determines the effects of posture on time up and go test. Half of the subjects will assume a high-power posture, while the other half will assume a low-power posture.

Read the detailed description

Subjects in the experimental group were instructed to stand with hands on their hips, elbows pointing out and feet approximately one foot apart for 20 seconds. Subjects in the control group were instructed to stand with hands and arms wrapping around the torso and feet together for 20 seconds. Timed Up and Go test was administered using an OmniVR™ Virtual Rehabilitation System before and after the postural intervention

Being tested
high-power, low-power

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • high-powerOther

    Subjects will stand with hands on their hips, elbows pointing out and feet approximately one foot apart (high-power) for 20 seconds.

  • low-powerOther

    Subjects will stand with hands and arms wrapping around the torso and feet together (low-power) for 20 seconds.

Study groups in NCT03032393
Study groupRoleWhat they receive
DominantExperimentalSubjects in the experimental group were instructed to stand with hands on their hips, elbows pointing out and feet approximately one foot apart for 20 seconds.
Receives: Other: high-power
SubmissiveActive comparatorSubjects in the control group were instructed to stand with hands and arms wrapping around the torso and feet together for 20 seconds.
Receives: Other: low-power

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Timed up and go Test

    Patients wear their regular footwear and can use a walking aid if needed. Begin by having the patient sit back in a standard arm chair and identify a line 3 meters or 10 feet away on the floor. The timed up and go test measures the amount of time, in seconds, that it takes to stand from a chair, walk 3 meters, turn around and walk back to the chair, and sit down again.

    A change between pre and post postural intervention is reported. The time point for pre intervention is at baseline. The time point for post intervention is immediately after the intervention.

    Measured: Up to 3 minutes during each Timed up and go Test. Twice (pre and post the postural intention) at the same session (day).

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted26 Jan 2017 (estimated)
  2. Study start3 Feb 2017
  3. Primary completion31 Dec 2017
  4. Study completion31 Dec 2017

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
30 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03032393
Sponsor's protocol ID
071-2017
Status last verified
Aug 2020
First submitted
20 Jan 2017
Last updated
10 Aug 2020
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing high-power and low-power in people with Healthy Volunteers, run by Youngstown State University at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 10 Aug 2020. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Yes. Results are posted in the registry (first posted 10 Aug 2020). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Timed up and go Test (time frame: Up to 3 minutes during each Timed up and go Test. Twice (pre and post the postural intention) at the same session (day).). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 10 Aug 2020.

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