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Workout on Wheels Internet Intervention (WOWii)

15 januari 2020 uppdaterad av: Baylor Research Institute

Project Workout on Wheels Internet Intervention (WOWii): Summative Evaluation With Randomized Clinical Trial

Project WOWii examines how useful and effective an online format is for helping people with SCI get more exercise over 4 months. Study participants will meet over Skype weekly for 16 weeks and work through weekly online modules to start and stick with an accessible and individualized exercise program. Participants will be compensated for their time to attend fitness testing and complete surveys before and just after the 16-week program.

Studieöversikt

Status

Avslutad

Betingelser

Detaljerad beskrivning

This study will gather empirical evidence of the effectiveness of WOWii intervention in promoting changes in exercise behavior, fitness, and perceptions of exercise over the 16 week intervention as well as 2 months later for individuals living with SCI. The study staff will assess effectiveness by measuring participants (a) time spent each week doing aerobic exercise by self-report and objective monitoring, (b) aerobic capacity to assess fitness changes, and (c) self-reported perceptions of exercise barriers and self-efficacy at baseline, 4 months, and 6 months.

Participants will be randomly assigned to an experimental (WOWii) or a wait-list control group in one of four cohorts over a two-year period. This was an effective strategy in our previous trial in helping us achieve the full sample size. We will use a blocked randomization procedure to assure equal distribution of those with paraplegia and tetraplegia. Four cohorts will be enrolled over two years, with each having up to 36 people. This allows for up to 18 participants in the experimental and control groups, which permits us to offer two different time options for participants to attend the weekly meetings, as our video conferencing software allows up to 10 people to participate in the group video chat. Each cohort will be divided into two groups of 18 study participants as experimental and wait-list control groups. The experimental group will be divided into two groups of nine participants. Each cohort will begin the intervention at the same time and attend weekly calls together. All participants will undergo a pre-screen assessment which includes eligibility assessment. Participants will undergo 2 in-person fitness testing assessments at baseline at the end of the 16 week internet intervention with online meetings, before or during which they will complete an online survey and follow. A third follow up assessment will be conducted as an online survey at 6 months, which is 2 months after the intervention is complete, and an exit survey will be conducted individually over the phone after within one week of completing the final online survey. The wait-list control group will be offered the intervention at the end of the 6 month period. Due to low enrollment numbers, we will likely add a 5th cohort for enrollment.

Studietyp

Interventionell

Inskrivning (Faktisk)

168

Fas

  • Inte tillämpbar

Kontakter och platser

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

Studieorter

    • Texas
      • Dallas, Texas, Förenta staterna, 75246
        • Baylor Institute for Rehabilitation

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 70 år (Vuxen, Äldre vuxen)

Tar emot friska volontärer

Ja

Kön som är behöriga för studier

Allt

Beskrivning

Inclusion Criteria:

  • Between the ages of 18 - 70 years old;
  • Have SCI > 6 months with the ability to use arms enough for arm-based exercise and requires wheelchair use;
  • Have access to a computer with internet access or if they do not have computer/internet access, have experience using a computer and going online;
  • Obtain physician signed approval to participate in the exercise study; and
  • Not be currently physically active, based on responses to the 7-item Behavioral Risk Factor Surveillance physical activity survey.

Exclusion Criteria:

  • Not receive physician approval to begin an exercise program;
  • Have participated in the previous pilot studies; and
  • Unable to read the English language.

Studieplan

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

Hur är studien utformad?

Designdetaljer

  • Primärt syfte: Förebyggande
  • Tilldelning: Randomiserad
  • Interventionsmodell: Parallellt uppdrag
  • Maskning: Ingen (Open Label)

Vapen och interventioner

Deltagargrupp / Arm
Intervention / Behandling
Experimentell: Intervention

Participants will self-monitor their exercise on the WOWii website, which has a page to record the type, duration, and intensity of daily exercise bouts.

Two devices will track participants' exercise, a Polar heart rate monitor (RS300X, Polar®), which will provide data on the day, duration, and intensity (average and maximum) of aerobic activity and an ActiGraph accelerometer (model GT3X), which detects movement in three planes to indicate frequency and intensity of movement throughout the day. Experimental participants will be provided a Polar heart rate monitor to wear during each exercise bout for the entire length of the 6-month study, and exercise data will be collected weekly.

Physiological outcomes on fitness will be assessed by measuring weight and aerobic capacity in a Cardiopulmonary Lab by a doctoral-trained physical therapist.

Participants will complete surveys to report on their exercise self-efficacy and perceived barriers.

Inget ingripande: Wait-List Control

Vad mäter studien?

Primära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Change in aerobic exercise (Participant adoption)
Tidsram: 16 weeks
minutes per week measured by Polar activity tracker (objective)
16 weeks
Aerobic exercise maintenance
Tidsram: 16 weeks
minutes per week measured by Polar activity tracker (objective)
16 weeks
Change in aerobic exercise (Participant adoption)
Tidsram: Baseline & 16 weeks
minutes per week measured by The International Physical Activity Questionnaire (IPAQ) (subjective)
Baseline & 16 weeks
Aerobic exercise maintenance
Tidsram: 16 weeks
minutes per week measured by The International Physical Activity Questionnaire (IPAQ) (subjective)
16 weeks

Sekundära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Change in aerobic fitness
Tidsram: Baseline & 16 weeks
peak V02 using continuous, graded arm crank protocol
Baseline & 16 weeks
Exercise Self-Efficacy
Tidsram: 16 weeks
health promotion scale with exercise subscale Self Rated Abilities for Health Practices Scale (SRAHP)
16 weeks
Change in perceived exercise barriers
Tidsram: Baseline & 16 weeks
Change in summary score of barriers on The Barriers to Health Activities among Disabled Persons scale (BHADP) from baseline to 16 weeks
Baseline & 16 weeks

Samarbetspartners och utredare

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

Utredare

  • Huvudutredare: Katherine Froehlich-Grobe, Ph.D., Baylor Institute for Rehabilitation

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)

6 juni 2017

Primärt slutförande (Faktisk)

1 oktober 2019

Avslutad studie (Faktisk)

31 december 2019

Studieregistreringsdatum

Först inskickad

9 juni 2017

Först inskickad som uppfyllde QC-kriterierna

14 juni 2017

Första postat (Faktisk)

16 juni 2017

Uppdateringar av studier

Senaste uppdatering publicerad (Faktisk)

18 januari 2020

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

15 januari 2020

Senast verifierad

1 januari 2020

Mer information

Termer relaterade till denna studie

Plan för individuella deltagardata (IPD)

Planerar du att dela individuella deltagardata (IPD)?

NEJ

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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