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Computer-vision Aided Community Back Pain Physiotherapy Services (CV)

20 maj 2021 uppdaterad av: Helen Dawes, Oxford Brookes University
Back pain affects one-third of the UK population every year with a huge impact on the health service and economy. The aim of this study is to test the validity of a computer-vision (CV) technology that uses cameras on phones/tablets/webcams to assess a person's movement and function with the ultimate goal to use the CV system to screen for back pain conditions. Participants with and without back pain will be included in the study and they will be asked to perform standard functional movements that would be used for a physiotherapy assessment for a back condition. The participants will also perform these movements in front of a camera for video recordings to be analysed by the CV system. The measurements by the CV system will be compared to the measurements by the physiotherapist. Additionally, participants will perform and record videos of the same set of movements at home to test the feasibility of the CV system in a home environment.

Studieöversikt

Status

Rekrytering

Betingelser

Detaljerad beskrivning

Back pain affects one-third of the UK population every year with a huge impact on the health service and economy. One specific back pain condition is Axial Spondyloarthropathy (AxSpa), which is an inflammatory spinal arthritis that causes pain and stiffness. This life-long condition presents in the early twenties as 'regular' back pain. Due to its similarity to other back pain conditions, there is an average 8.5-year delay to diagnosis. The aim of this study is to test the validity of a computer-vision (CV) technology that uses cameras on phones/tablets/webcams to assess a person's movement and function with the ultimate goal to use the CV system to screen for back pain conditions, such as AxSpa. The CV system development is led by the GoodBoost Wellbeing Limited and The National Axial Spondyloarthritis Society (NASS) is supporting the recruitment of people living with AxSpa.

The CV system that has been developed is a form of artificial intelligence video analysis which is able to automatically measure specific functional movements captured on video. To validate this CV system, this study is designed to compare it to the clinical gold standard measurement by a physiotherapist. Participants with and without back pain will be included in the study and they will be asked to perform standard functional movements that would be used for a physiotherapy assessment for a back condition. The participants will also perform these movements in front of a camera for video recordings to be analysed by the CV system. The measurements by the CV system will be compared to the measurements by the physiotherapist. Additionally, participants will perform and record videos of the same set of movements at home to test the feasibility of the CV system in a home environment.

Studietyp

Observationell

Inskrivning (Förväntat)

100

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studiekontakt

Studera Kontakt Backup

Studieorter

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

18 år till 100 år (Vuxen, Äldre vuxen)

Tar emot friska volontärer

Nej

Kön som är behöriga för studier

Allt

Testmetod

Icke-sannolikhetsprov

Studera befolkning

Healthy participants and participants with non-specific back pain will be recruited via advertisement through networks associated with the research team members. Participants with AxSpa will initially be recruited from the Oxford area by The National Axial Spondyloarthritis Society (NASS) promotion.

Beskrivning

Inclusion Criteria:

  • ● The participant is willing and able to give informed consent for participation in the study.

    • Male or Female, aged 18 years or above.
    • For back pain group: diagnosed with AxSpa or long-standing non-specific LBP
    • For healthy group: healthy with no long-standing back pain
    • For the home setting, the participant must be capable of uploading videos from a smartphone or webcam.

Exclusion Criteria:

  • ● Has had surgery within 6 months of registration

    • Unable to stand independently
    • Unable to pass screening questions to participate in physical activity
    • Serious neurological condition preventing normal movement or walking ability
    • Any severe medical conditions, such as cardiovascular disease

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

  • Observationsmodeller: Case-Control
  • Tidsperspektiv: Blivande

Kohorter och interventioner

Grupp / Kohort
Back pain and no back pain
Participants with and without back pain will be included in the study and they will be asked to perform standard functional movements that would be used for a physiotherapy assessment for a back condition. The participants will also perform these movements in front of a camera for video recordings to be analysed by the CV system. The measurements by the CV system will be compared to the measurements by the physiotherapist. Additionally, participants will perform and record videos of the same set of movements at home to test the feasibility of the CV system in a home environment.

Vad mäter studien?

Primära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Primary movement Lumbar spine lateral flexion
Tidsram: 1 minute
Concurrent validity of lumbar spine lateral flexion measurement by the CV system compared to physiotherapy measurement.
1 minute

Sekundära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Movement of Lumbar global flexion
Tidsram: 1 minute
Concurrent validity of: Lumbar global flexion measurement by the CV system compared to physiotherapy measurement.
1 minute
Movement of Cervical rotation
Tidsram: 1 minute
Concurrent validity of: Cervical rotation seated measurement by the CV system compared to physiotherapy measurement.
1 minute
Movement of Hip internal rotation
Tidsram: 1 minute
Concurrent validity of: Hip internal rotation seated measurement by the CV system compared to physiotherapy measurement.
1 minute
Movement of Hip abduction
Tidsram: 1 minute
Concurrent validity of: Hip abduction standing measurement by the CV system compared to physiotherapy measurement.
1 minute
Movement of Shoulder flexion
Tidsram: 1 minute
Concurrent validity of: Shoulder flexion measurement by the CV system compared to physiotherapy measurement.
1 minute
Movement 6
Tidsram: 1 minute
Concurrent validity of: Chest expansion measurement by the CV system compared to physiotherapy measurement.
1 minute
Movement of Sit-to-stand
Tidsram: 1 minute
Concurrent validity of Sit-to-stand measurement by the CV system compared to physiotherapy measurement.
1 minute
Standing posture spinal kyphosis
Tidsram: 1 minute
Posture as measured by spinal kyphosis
1 minute
Standing posture tragus to ear
Tidsram: 1 minute
Posture as measured by tragus to walk
1 minute
Leg strength
Tidsram: 1 minute
5 time sit to stand
1 minute

Samarbetspartners och utredare

Det är här du hittar personer och organisationer som är involverade i denna studie.

Sponsor

Oxford Brookes University

Samarbetspartners

Good Boost Wellbeing
National Axial Spondyloarthritis Society

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart (Faktisk)

1 april 2021

Primärt slutförande (Förväntat)

1 januari 2022

Avslutad studie (Förväntat)

1 juni 2022

Studieregistreringsdatum

Först inskickad

15 maj 2021

Först inskickad som uppfyllde QC-kriterierna

19 maj 2021

Första postat (Faktisk)

20 maj 2021

Uppdateringar av studier

Senaste uppdatering publicerad (Faktisk)

24 maj 2021

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

20 maj 2021

Senast verifierad

1 maj 2021

Mer information

Termer relaterade till denna studie

Nyckelord

Ytterligare relevanta MeSH-villkor

Andra studie-ID-nummer

  • 201429

Plan för individuella deltagardata (IPD)

Planerar du att dela individuella deltagardata (IPD)?

Nej

IPD-planbeskrivning

Direct access will be granted to authorised representatives from the Sponsor and host institution for monitoring and/or audit of the study to ensure compliance with regulations.

Läkemedels- och apparatinformation, studiedokument

Studerar en amerikansk FDA-reglerad läkemedelsprodukt

Nej

Studerar en amerikansk FDA-reglerad produktprodukt

Nej

Denna information hämtades direkt från webbplatsen clinicaltrials.gov utan några ändringar. Om du har några önskemål om att ändra, ta bort eller uppdatera dina studieuppgifter, vänligen kontakta register@clinicaltrials.gov. Så snart en ändring har implementerats på clinicaltrials.gov, kommer denna att uppdateras automatiskt även på vår webbplats .

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