NCT06294223

Brief Summary

The aim of this study was to measure the acute change in oxygen saturation of skeletal muscle during resistance exercise in the upper extremity using near-infrared spectroscopy.

Trial Health

57
Monitor

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
30

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Mar 2024

Geographic Reach
1 country

1 active site

Status
recruiting

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

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

February 20, 2024

Completed
10 days until next milestone

Study Start

First participant enrolled

March 1, 2024

Completed
4 days until next milestone

First Posted

Study publicly available on registry

March 5, 2024

Completed
12 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 1, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

March 1, 2025

Completed
Last Updated

March 18, 2024

Status Verified

March 1, 2024

Enrollment Period

1 year

First QC Date

February 20, 2024

Last Update Submit

March 15, 2024

Conditions

Keywords

Near-infrared SpectroscopyResistance ExerciseExercise IntensityMuscle OxygenationMuscle Activation

Outcome Measures

Primary Outcomes (4)

  • Determination of Blood Pressure

    Systolic/diastolic blood pressure will be determined with a digital blood pressure monitor and will be recorded in mmHg. Measurements will be taken via the right brachial artery in a comfortable position.

    Measurement will be made before and immediately after exercise.

  • Saturation Measurement

    Oxygen saturation will be measured with a pulse oximeter device and recorded on the form.

    Measurement will be made before and immediately after exercise.

  • Muscle Oxygenation Measurement

    MOXY Pro (Moxy 3, Firmware 1.1 Hutchinson MN, USA), a near-infrared spectroscopy device, will be used to measure the muscle oxygen rate (SmO2) and total hemoglobin amount (tHb) of the biceps brachii muscle.

    Baseline.

  • Determination of Heart Rate

    Heart rate will be determined with a digital blood pressure monitor and will be recorded in BPM.

    Measurement will be made before and immediately after exercise.

Study Arms (1)

Measurement of Upper Extremity Muscle Oxygenation

EXPERIMENTAL

Measuring muscle oxygenation with fatigue protocol.

Device: Exercise follow up with near-infrared spectroscopy

Interventions

Exercises will be followed by near-infrared spectroscopy. Fatigue protocol will be applied.

Measurement of Upper Extremity Muscle Oxygenation

Eligibility Criteria

Age18 Years - 30 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • Volunteering to participate in the study
  • Being over 18 years old
  • Having a Body Mass Index (BMI) value between 23-30 kg/m2
  • Absence of comorbid disease of the orthopedic, neurological, cardiopulmonery system

You may not qualify if:

  • Smoking / alcohol use
  • Presence of orthopedic disease effecting the upper extremity or previous surgery
  • Presence of cardiopulmonery disease that prevents exercise
  • Participants who performed resistance exercise regulary for more than 6 months

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Saglik Bilimleri University

Istanbul, 34010, Turkey (Türkiye)

RECRUITING

MeSH Terms

Interventions

Spectroscopy, Near-Infrared

Intervention Hierarchy (Ancestors)

Diagnostic ImagingDiagnostic Techniques and ProceduresDiagnosisSpectrum AnalysisChemistry Techniques, AnalyticalInvestigative Techniques

Study Officials

  • Esra Pehlivan, Ass. Prof.

    Saglik Bilimleri Universitesi

    STUDY DIRECTOR
  • Mehmet Burak Uyaroğlu, Pt.PhD(c)

    Saglik Bilimleri Universitesi

    PRINCIPAL INVESTIGATOR
  • Tuna Sümer, PT

    Saglik Bilimleri Universitesi

    STUDY CHAIR
  • Melisa Eren, PT

    Saglik Bilimleri Universitesi

    STUDY CHAIR
  • Ceren Balıkcı, PT

    Saglik Bilimleri Universitesi

    STUDY CHAIR

Central Study Contacts

Esra Pehlivan, Ass. Prof

CONTACT

Tuna Sümer, PT

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
TREATMENT
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
PT

Study Record Dates

First Submitted

February 20, 2024

First Posted

March 5, 2024

Study Start

March 1, 2024

Primary Completion

March 1, 2025

Study Completion

March 1, 2025

Last Updated

March 18, 2024

Record last verified: 2024-03

Data Sharing

IPD Sharing
Will not share

Locations