Track this trial free. DataLookout checks ClinicalTrials.gov daily and emails you which fields changed on NCT00265525 (status, enrollment, completion dates, endpoints, sites) when this record is updated. Free accounts track up to 5 trials.

Track this trial

Evaluation of a Web-based Intervention to Promote Physical Activity in Patients With Heart Disease.

StatusCompleted
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗

Amendment history

  1. Notable

    Phase: Phase 3 to Not applicable

    Results first posted: Jun 30, 2026; Primary endpoint revised; Secondary endpoints: 10 to 2

    Show what changed: Primary endpoints
    Physical activityActivity: measuredMeasured at baselineBaseline (dayDay of hospitalHospital dischargeDischarge), 6 monthsMonths and 12 monthsMonths via:Via Pedometer
    Show what changed: Secondary endpoints
    MeasuredModerate ator baseline,Vigorous 6Physical months, and 12 months via follow-up questionnaire: Recurrent cardiac events Barriers Task Self-efficacy Outcome expectations Social Support Perceived environmentActivity Heart diseaseDisease specificHealth-related qualityQuality of life Use of secondary prevention medications Pedometer (9days)Life

    Study Status, Sponsor/Collaborators, Study Design, Outcome Measures, Participant Flow, Baseline Characteristics, Outcome Measures (Results), Adverse Events, Limitations and Caveats, More Informationv8

  2. Minor

    Study Status, Study Design

    Re-verified, no change to tracked fields

    v7

  3. Minor

    Interventions: CardioFit (Behavioral), Usual care (Behavioral) to CardioFit (Behavioral)

    Study Status, Arms and Interventionsv6

  4. Minor

    Study Identification, Study Status, References

    v5

  5. Notable

    Primary endpoints: 4 to 1

    Trial status: Recruiting to Completed; Enrollment target: 304 to 223; Primary completion date: Jun 2007; and 5 more

    Show all 9 changes in this update
    • Notable Primary endpoints: 4 to 1
      Show what changed
      7 day Physical Activity recall, and Godin Leisure Time Exercise Questionnaire, Pedometer (9 day)
    • Minor Trial status: Recruiting to Completed
    • Minor Enrollment target: 304 to 223
    • Minor Primary completion date: Jun 2007
    • Minor Study completion date changed from estimate of Jun 2007 to Aug 2007
    • Minor Secondary endpoints: 9 to 10
      Show what changed
      Use of secondary prevention medications Pedometer (measured at 12 months via follow-up questionnaire9days)
    • Minor Site details revised at 2 of 2 sites
    • Minor Collaborator revised
      Show what changed
      Heart and Stroke Foundation of CanadaOntario
    • Minor Study arms: 0 to 2

    Study Status, Sponsor/Collaborators, Oversight, Study Design, Arms and Interventions, Outcome Measures, Contacts/Locationsv4

Show 2 earlier versions

  1. Minor

    Study Status

    Re-verified, no change to tracked fields

    v3

  2. Notable

    Primary endpoints revised (4)

    Secondary endpoints revised (9)

    Show what changed: Primary endpoints
    1. 7 day Physical Activity recall, and 2. Godin Leisure Time Exercise Questionnaire, 3. Pedometer (9 day)
    Show what changed: Secondary endpoints
    1. Recurrent cardiac events 2. Barriers 3. Task Self-efficacy 4. Outcome expectations 5. Social Support 6. Perceived environment 7. Heart disease specific quality of life 8. Use of secondary prevention medications (measured at 12 months via follow-up questionnaire)

    Study Status, Outcome Measuresv2

  1. Minor

    Study First Submitted

  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
A randomized control trial (RCT) is planned to evaluate a web-based intervention (CardioFit) against usual care in increasing physical activity levels in patients with Coronary Artery Disease (CAD). We hypothesize that compared to usual care, participants in CardioFit will; a) have increased physical activity levels, b) will have a higher health-related quality of life at measurement dates and, c) will have greater improvements in psychosocial predictors.
Trial Details
NCT Number NCT00265525
Lead Sponsor Ottawa Heart Institute Research Corporation
Collaborators: Heart and Stroke Foundation of Ontario
Conditions Coronary Artery Disease (CAD)
Enrollment 223 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov