- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT07699848
Active Versus Passive Sitting, Cognition and Energy
18. august 2026 opdateret af: Joseph Signorile, University of Miami
Differences in Muscle Utilization, Tissue Pressure, Cognitive Performance, and Caloric Output Among Active and Passive Sitting Positions.
The study will compare cognitive capacity, muscle utilization patterns, soft tissue seated pressure and caloric output during four seated conditions:
- passive sitting in a regular chair;
- passive sitting in an exercise chair;
- sitting in the exercise chair during active dynamic exercise; and,
- sitting in the chair during active static exercise.
Studieoversigt
Status
Rekruttering
Betingelser
Undersøgelsestype
Interventionel
Tilmelding (Anslået)
35
Fase
- Ikke anvendelig
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiekontakt
- Navn: Ethan J Elkins, MS
- Telefonnummer: 3052844173
- E-mail: exe453@miami.edu
Undersøgelse Kontakt Backup
- Navn: Joseph Signorile J Joseph Signorile, PhD
- Telefonnummer: 3058981458
- E-mail: jsignorile@miami.edu
Studiesteder
-
-
Florida
-
Coral Gables, Florida, Forenede Stater, 33146
- Rekruttering
- Laboratory of Neuromuscular Research and Active Aging
-
Kontakt:
- Ethan J Elkins, MS
- Telefonnummer: 3052844173
- E-mail: exe453@miami.edu
-
Kontakt:
- Joseph Signorile Joseph Signorile, PhD
- Telefonnummer: 305-898-1458
- E-mail: jsignorile@miami.edu
-
-
Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
- Voksen
- Ældre voksen
Tager imod sunde frivillige
Ja
Beskrivelse
Inclusion Criteria:
- Adult (18-70)
Exclusion Criteria:
- Any current injury in the lower limb or trunk.
- Use of prescription drugs or supplements that may affect cardiovascular or neuromuscular responses.
- Reported lack of sleep or stress that may affect physiological responses to exercise.
- Cardiovascular, respiratory, neurologic, balance, metabolic, or musculoskeletal conditions that could increase risk during exercise testing
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Grundvidenskab
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Ingen indgriben: Passive Comparator: Traditional Chair
Participant will sit in the traditional chair for the amount of time it takes them to read a scientific article.
|
|
|
Placebo komparator: Passive Comparator: Exercise Chair
Participant will sit in the exercise chair for the amount of time it takes them to read a scientific article.
|
A chair-based exercise program using a specialized chair that allows participants to lift their body weight.
|
|
Eksperimentel: Experimental: Dynamic Leg Exercise in Exercise Chair
Participant will sit in the exercise chair for the amount of time it takes them to read a scientific article while actively pushing down and releasing the foot operated lever as many times as possible.
|
A chair-based exercise program performed using a specialized exercise chair equipped with a foot-operated lever.
Participants repeatedly depress and release the foot-operated lever during the intervention period.
|
|
Eksperimentel: Experimental: Static Leg Exercise in Exercise Chair
Participant will sit in the exercise chair for the amount of time it takes them to read a scientific article while actively pushing down and holding the foot operated lever.
|
A chair-based exercise program performed using a specialized exercise chair equipped with a foot-operated lever.
Participants depress and maintain pressure on the foot-operated lever during the intervention period.
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Differences in cognitive performance among chair conditions as measured by the Psychomotor Vigilance Test in number of key depressions
Tidsramme: Approximately 3 minutes
|
Cognitive performance will be assessed using the 3-minute Psychomotor Vigilance Test (PVT).
During the test, participants will press the space bar as quickly as possible in response to the appearance of a visual stimulus on a computer screen.
Performance will be measured as the total number of valid responses recorded during the test.
Higher values indicate greater alertness, sustained attention, and reaction speed.
|
Approximately 3 minutes
|
|
Executive function among chair conditions as measured by the Stroop Test using words counted.
Tidsramme: Approximately 5 minutes.
|
Executive function will be assessed using the Stroop Test, a cognitive task requiring participants to respond to color word stimuli.
The outcome will be measured by total words counted, reported as the number of words.
|
Approximately 5 minutes.
|
|
Executive function among chair conditions as measured by the Stroop Test using error rate.
Tidsramme: Approximately 5 minutes.
|
Executive function will be assessed using the Stroop Test, a cognitive task requiring participants to respond to color word stimuli.
The outcome will be measured by error rate, reported as the percentage of errors.
|
Approximately 5 minutes.
|
|
Muscle activity among chair conditions using electromyography
Tidsramme: Approximately 45 minutes
|
Muscle activity will be assessed using surface electromyography (EMG).
Muscle activation will be quantified as EMG amplitude, measured in microvolts (µV) from EMG recordings.
Higher values indicate greater muscle activity.
|
Approximately 45 minutes
|
|
Peak seated tissue pressure among chair conditions using a pressure sensitive mat
Tidsramme: Approximately 15 minutes
|
Seated tissue pressure will be assessed using a pressure-sensitive mat placed on the seat surface of each chair.
Peak pressure will be recorded to quantify the highest pressure exerted at the seating interface during each chair condition, measured in kilopascals.
Higher values indicate greater localized pressure on seated tissues.
|
Approximately 15 minutes
|
|
Metabolic cost of sitting among the chair conditions using a portable oxygen consumption unit
Tidsramme: Approximately 25 minutes
|
Metabolic cost during sitting will be assessed under each chair condition using a portable indirect calorimetry device.
Participants will wear a facemask that measures oxygen consumption (VO₂) and carbon dioxide production (VCO₂).
These measurements will be used to estimate energy expenditure during the sitting period.
Higher values indicate greater metabolic cost.
|
Approximately 25 minutes
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Samarbejdspartnere
Efterforskere
- Ledende efterforsker: Joseph J Signorile, PhD, University of Miami - Coral Gables Campus
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart (Faktiske)
23. juni 2026
Primær færdiggørelse (Anslået)
30. september 2027
Studieafslutning (Anslået)
30. september 2027
Datoer for studieregistrering
Først indsendt
7. juli 2026
Først indsendt, der opfyldte QC-kriterier
7. juli 2026
Først opslået (Faktiske)
13. juli 2026
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
20. august 2026
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
18. august 2026
Sidst verificeret
1. august 2026
Mere information
Begreber relateret til denne undersøgelse
Andre undersøgelses-id-numre
- 20260691
- FP00021633 (Andet bevillings-/finansieringsnummer: Robot Studios)
Plan for individuelle deltagerdata (IPD)
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