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Use of Wearable Tech to Increase Physical Activity in Inpatient Rehabilitation for Patients With Chronic Pain

24. januar 2020 opdateret af: Norwegian University of Science and Technology
The aim of this project is to evaluate whether use of wearable tech increases levels of physical activity in patients participating in inpatient rehabilitation for chronic pain.

Studieoversigt

Status

Afsluttet

Betingelser

Intervention / Behandling

Detaljeret beskrivelse

Chronic pain is a vast problem with profound consequences for individuals and societies. Exercise and physical activity is an important part of the treatment for chronic pain. Use of wearable tech might be a way to help facilitate physical activity in patients with chronic pain. Here it will be evaluated whether use of wearable tech giving feedback about the user's activity level increases physical activity in patients participating in inpatient rehabilitation for chronic pain. The control group will be wearing the same wearable tech as the intervention group, but they will not receive any feedback about their activity level.

The feedback application will give participants in the intervention group information about the number of PAI they earn each week. PAI is short for personal activity Intelligence. You earn PAI points every time your heart rate increases: The higher heart rate, the faster you earn PAI. Previous research have shown that those who achieve 100 PAI or more every week over time live for an average of more than eight years longer than others.

During the study all participants will take part in a traditional inpatient rehabilitation program. The program consist of two periods at the rehabilitation center with two weeks at home in-between. The study will take place during the two periods at the senter and the period at home. Time spent on physical activity and number of earned PAI's will be counted during the period at home.

Undersøgelsestype

Interventionel

Tilmelding (Faktiske)

44

Fase

  • Ikke anvendelig

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiesteder

  • Norge
      • Rissa, Norge
        • Unicare Helsefort

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

18 år og ældre (Voksen, Ældre voksen)

Tager imod sunde frivillige

Ingen

Køn, der er berettiget til at studere

Alle

Beskrivelse

Inclusion Criteria:

  • taking part in inpatient rehabilitation at Unicare Helefort Rehabilitation center for chronic pain.

Exclusion Criteria:

  • not having a smartphone (will not be able to access the mobile application).
  • using a wheelchair (the technology will be not able to measure activity correctly)

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Behandling
  • Tildeling: Randomiseret
  • Interventionel model: Parallel tildeling
  • Maskning: Enkelt

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Aktiv komparator: Bærbar teknologi uden feedback
Denne gruppe vil bære det samme aktivitetsmåleapparat som interventionsgruppen, men de vil ikke modtage feedback om deres aktivitetsniveau. De vil ikke have adgang til mobilapplikationen. De vil deltage i det samme rehabiliteringsprogram som indsatsgruppen.
Adfærdsmæssigt: Rehabilitation program
traditional inpatient rehabilitation program.
Enhed: Wearable tech without feedback
An armwrist device measuring physical activity level, no reporting back to the user.
Eksperimentel: Wearable tech with feedback
This group will be wearing an activity measurement device (wristband) and receive feedback about their activity level through a mobile application while taking part in a traditional inpatient rehabilitation program for patients with chronic pain.
Enhed: Wearable tech with feedback
An armwrist device measuring physical activity level. The user will receive information about their physical activity level through their smartphone.
Adfærdsmæssigt: Rehabilitation program
traditional inpatient rehabilitation program.

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Activity level
Tidsramme: 2 weeks (time period at home between two stays at the rehabilitation center)
Time spent in moderate to vigorous physical activity (minutes per day)
2 weeks (time period at home between two stays at the rehabilitation center)
Number of PAIs
Tidsramme: 2 weeks (time period at home between two stays at the rehabilitation center)
mean number of Personal Activity Intelligence (PAI) points achieved per week
2 weeks (time period at home between two stays at the rehabilitation center)
Percentage achieving 100 PAIs per week
Tidsramme: 2 weeks (time period at home between two stays at the rehabilitation center)
Personal Activity Intelligence (PAI)
2 weeks (time period at home between two stays at the rehabilitation center)

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
oxygen uptake
Tidsramme: 6 weeks (from inclusion to end of rehabilitation program)
submaximal oxygen uptake measured by the Åstrand bicycle test (described in Textbook of work physiology by Astrand from 1986)
6 weeks (from inclusion to end of rehabilitation program)
Anxiety and depression symptoms
Tidsramme: 6 weeks (from inclusion to end of rehabilitation program)
HSCL-25 questionnaire
6 weeks (from inclusion to end of rehabilitation program)
Average pain
Tidsramme: 6 weeks (from inclusion to end of rehabilitation program)
Visual Analogue Scale (VAS). VAS is a straight horizontal line where the ends are defined as the extreme limits from the left (0-no pain) to the right (100-worst imaginable pain). The patient is asked to mark his pain level on the line between the two endpoints. The distance between 'no pain at all' and the mark then defines the subject's pain.
6 weeks (from inclusion to end of rehabilitation program)
Health related quality of life
Tidsramme: 6 weeks (from inclusion to end of rehabilitation program)
EQ5D questionnaire
6 weeks (from inclusion to end of rehabilitation program)
Body weight
Tidsramme: 6 weeks (from inclusion to end of rehabilitation program)
body weight in kilograms
6 weeks (from inclusion to end of rehabilitation program)
Body Mass Index score
Tidsramme: 6 weeks (from inclusion to end of rehabilitation program)
weight in kilograms divided by height in metres squared
6 weeks (from inclusion to end of rehabilitation program)

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Sponsor

Norwegian University of Science and Technology

Efterforskere

  • Ledende efterforsker: Lene Aasdahl, PhD MD, National Taiwan Normal University
  • Studieleder: Jorunn Helbostad, Dr Philos, Norwegian University of Science and Technology

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)

8. august 2019

Primær færdiggørelse (Faktiske)

14. januar 2020

Studieafslutning (Faktiske)

14. januar 2020

Datoer for studieregistrering

Først indsendt

22. juli 2019

Først indsendt, der opfyldte QC-kriterier

22. juli 2019

Først opslået (Faktiske)

24. juli 2019

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

27. januar 2020

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

24. januar 2020

Sidst verificeret

1. januar 2020

Mere information

Begreber relateret til denne undersøgelse

Nøgleord

Yderligere relevante MeSH-vilkår

Andre undersøgelses-id-numre

  • 2019/800

Plan for individuelle deltagerdata (IPD)

Planlægger du at dele individuelle deltagerdata (IPD)?

INGEN

Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter

Studerer et amerikansk FDA-reguleret lægemiddelprodukt

Ingen

Studerer et amerikansk FDA-reguleret enhedsprodukt

Ingen

Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .

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