The Effects of Standardized vs Individualized Seat Height on 1-minute Sit-to-stand Performance (ESTI-STS)

November 6, 2022 updated by: University of Zurich

The 1-minute sit-to-stand test (1MSTS) is a widely used functional capacity test and has promising predictive potential. Current standards of practice suggest the use of a chair with a standardized height. However, this practice makes the test more demanding for taller individuals than for shorter individuals. This implies over- or underestimation of functional capacity depending on body morphology.

Therefore, the aim of this study is to investigate the influence of knee joint angle, femur length and bodyweight on the 1MSTS performance in healthy subjects with different morphology.

Study Overview

Detailed Description

This is a randomized cross-over trial with the participants performing both procedures twice in one visit. Sufficient breaks in between the tests is granted.

Study Type

Observational

Enrollment (Actual)

30

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Zurich, Switzerland, 8091
        • University Hospital Zurich

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

Healthy individuals

Description

Inclusion Criteria:

  • Informed consent as documented by signature
  • Age 18 and older
  • Healthy
  • Ability to conduct a 1-minute sit-to-stand-test
  • Ability to follow study procedures and instructions in German

Exclusion Criteria:

  • Known cardiopulmonary or metabolic diseases (e.g., heart disease, diabetes mellitus etc.)
  • Smoking (ex-smoker allowed; if they stopped smoking at least one year before the study inclusion)
  • Physical or intellectual impairment precluding informed consent or protocol adherence
  • Respiratory infection in the last two weeks
  • Pain during sit-to-stand movement

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Observational Models: Other
  • Time Perspectives: Cross-Sectional

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Repetitions in the 1-minute sit-to-stand test
Time Frame: Day 1
Comparison between the procedures
Day 1

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Predictors towards performance in the 1-minute sit-to-stand test
Time Frame: Day 1
Comparison between the procedures
Day 1

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

April 20, 2021

Primary Completion (Actual)

November 3, 2022

Study Completion (Actual)

November 3, 2022

Study Registration Dates

First Submitted

February 21, 2021

First Submitted That Met QC Criteria

February 25, 2021

First Posted (Actual)

February 26, 2021

Study Record Updates

Last Update Posted (Actual)

November 8, 2022

Last Update Submitted That Met QC Criteria

November 6, 2022

Last Verified

November 1, 2022

More Information

Terms related to this study

Other Study ID Numbers

  • 2020-02945

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

Undecided

IPD Plan Description

On reasonable request

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Healthy Individuals

Clinical Trials on Standardized 1-minute sit-to-stand test

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