NCT06308042

Brief Summary

This study aimed to demonstrate the remote reliability of the 30-second sit-to-stand test in patients with multiple sclerosis.

Trial Health

35
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
10

participants targeted

Target at below P25 for all trials

Timeline
Completed

Started Mar 2024

Shorter than P25 for all trials

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

March 6, 2024

Completed
5 days until next milestone

Study Start

First participant enrolled

March 11, 2024

Completed
2 days until next milestone

First Posted

Study publicly available on registry

March 13, 2024

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 24, 2024

Completed
5 days until next milestone

Study Completion

Last participant's last visit for all outcomes

June 29, 2024

Completed
Last Updated

March 13, 2024

Status Verified

March 1, 2024

Enrollment Period

4 months

First QC Date

March 6, 2024

Last Update Submit

March 6, 2024

Conditions

Keywords

30 SECONDS SIT AND STAND TESTREMOTE RELIABILITY

Outcome Measures

Primary Outcomes (1)

  • 30 second sit and stand test

    The 30-second sit-to-stand test is a test used to evaluate lower extremity muscle strength, balance and walking functions.

    24-48 hours

Interventions

The individual sits in the middle of the chair with his back upright, his feet on the ground, and his arms crossed in front of his chest. The individual starts the test with the start command while in this position and takes off as fully as he can for 30 seconds.

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

multiple sclerosis patients

You may qualify if:

  • Having been diagnosed with MS according to the McDonald criteria by a neurologist
  • having and being able to use a device with Internet access (e.g. smartphone, computer or tablet)
  • having EDSS between 1.5 and 6.5,
  • being between the ages of 18-65.

You may not qualify if:

  • Patients who have had a recurrence of the disease in the last 30 days,
  • have an additional health problem (orthopedic, neurological, internal or cardiorespiratory) that prevents standing/walking,
  • do not agree to participate in the study.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Multiple Sclerosis

Interventions

4-Acetamido-4'-isothiocyanatostilbene-2,2'-disulfonic Acid

Condition Hierarchy (Ancestors)

Demyelinating Autoimmune Diseases, CNSAutoimmune Diseases of the Nervous SystemNervous System DiseasesDemyelinating DiseasesAutoimmune DiseasesImmune System Diseases

Intervention Hierarchy (Ancestors)

StilbenesBenzylidene CompoundsBenzene DerivativesHydrocarbons, AromaticHydrocarbons, CyclicHydrocarbonsOrganic ChemicalsIsothiocyanatesIsocyanatesSulfur Compounds

Study Officials

  • Burcu talu

    Inonu University

    STUDY DIRECTOR

Central Study Contacts

DILAN DEMİRTAŞ KARAOBA

CONTACT

: BUSRA CANDIRI

CONTACT

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Associate professor, physiotherapist,

Study Record Dates

First Submitted

March 6, 2024

First Posted

March 13, 2024

Study Start

March 11, 2024

Primary Completion

June 24, 2024

Study Completion

June 29, 2024

Last Updated

March 13, 2024

Record last verified: 2024-03

Data Sharing

IPD Sharing
Will share

Study data can be shared with other researchers if desired

Shared Documents
STUDY PROTOCOL, SAP, CSR
Time Frame
After the study was published
Access Criteria
If requested from the authors, it can be shared with researchers at the authors' discretion.