- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT05034302
Posture Analysis Through Machine Learning (PathML)
Studienübersicht
Status
Bedingungen
Detaillierte Beschreibung
This is a cross-sectional, single observation study. Individuals will be drawn from local surrounding clinics and the general community. All recruitment will include both men and women. Selection criteria include individuals between the ages of 18-85 years, no major chronic illness that impair mobility and able to complete activities of daily living without assistance. Participants will complete one three hour session where there will be one video camera set up within the home (i.e., static cameras). For approximately 30 minutes of the session they will complete a semi-scripted routine that will include sit to stand transitions, a timed up and go test, and scripted activities of daily living.
Researchers will use a video camera to record participant behavior within their daily life. For two of the three hours, researchers will be video recordings the participants normal (unscripted) activities. • For one hour of the session we will use two cameras, one that will be held by a researcher and one that will be set up on a tripod. During this hour we will ask participants to follow a semi-structured protocol:
- 10 minutes recording the empty space
- 10 minutes that include a timed up a go test (sit up from a chair and walk 10 feet), repeat the test 3 times.
- 6 minute walk test (walk continuously for 6 minutes)
- Four stage balance test
- The remainder of the time, participants will complete standard activities of daily living like household chores, eating or drinking.
Data will be annotated using an established behavioral observation software by training research assistants (ground-truth). The image data from videos will be used to train machine learning models to classify physical activities (e.g. ,'walking', 'sitting' or 'standing up"), information about behavior (e.g., location and purpose of the activity), and performance (e.g., walking speed and sit to stand transition times).
Studientyp
Einschreibung (Tatsächlich)
Kontakte und Standorte
Studienorte
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California
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San Luis Obispo, California, Vereinigte Staaten, 93407
- CalPoly
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Teilnahmekriterien
Zulassungskriterien
Studienberechtigtes Alter
Akzeptiert gesunde Freiwillige
Studienberechtigte Geschlechter
Probenahmeverfahren
Studienpopulation
Beschreibung
Inclusion Criteria:
- Age 18-85 years
- No major chronic illness that impair mobility
- Able to complete activities of daily living without assistance.
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
Kohorten und Interventionen
Gruppe / Kohorte |
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Recordings
Selection criteria include individuals between the ages of 18-85 years, no major chronic illness that impair mobility and able to complete activities of daily living without assistance.
We will recruit approximately equal number of men and women and 30% of the sample will be racial or ethnic minorities.
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Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
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Postural Status
Zeitfenster: Upon enrollment (one timepoint)
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Sitting versus standing versus moving
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Upon enrollment (one timepoint)
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Activity type
Zeitfenster: Upon enrollment (one timepoint)
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Indoor vs outdoor vs driving
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Upon enrollment (one timepoint)
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Sit to stand transition time
Zeitfenster: Upon enrollment (one timepoint)
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Time it takes to go from sitting to standing
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Upon enrollment (one timepoint)
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Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
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Activity intensity
Zeitfenster: Upon enrollment (one timepoint)
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Sedentary, light, moderate and vigorous intensity
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Upon enrollment (one timepoint)
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Activity type
Zeitfenster: Upon enrollment (one timepoint)
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lying, sitting, driving, standing, housework or office work, walking, running, sports, other
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Upon enrollment (one timepoint)
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Mitarbeiter und Ermittler
Sponsor
Ermittler
- Hauptermittler: Sarah Keadle, Cal Poly
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn (Tatsächlich)
Primärer Abschluss (Voraussichtlich)
Studienabschluss (Voraussichtlich)
Studienanmeldedaten
Zuerst eingereicht
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst gepostet (Tatsächlich)
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Zuletzt verifiziert
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Schlüsselwörter
Andere Studien-ID-Nummern
- PathML2021
Plan für individuelle Teilnehmerdaten (IPD)
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Arzneimittel- und Geräteinformationen, Studienunterlagen
Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt
Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt
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