CClinicalTrials.gg
Status unknownNCT03207113Updated Oct 12, 2017

Adoption, Acceptability, and Effectiveness of a Mobile Health App for Personalised Prostate Cancer Survivorship Care.

An interventional study of Ned in Prostate Cancer, sponsored by Centre for Global eHealth Innovation. Status unknown at 1 site in Canada. Open to male participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2017-10-12.

Sponsored by Centre for Global eHealth Innovation · Not applicable, Interventional, and Supportive care

The sponsor has not verified this record recently (last verified Oct 2017), so the status shown — last known as Recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
610
Allocation
Not applicable
Ages
18 Years and older
Sex
Male
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Study summary

The Ned case study is a 12-month mixed methods embedded single-case study with a nested within-group pre-post comparison of health outcomes. 400 patients, 200 caregivers, and 10 clinicians will be given access to Ned. Participants will be asked to complete study assessments at baseline, 2 months, 6 months and 12 months. 30 semi-structured qualitative interviews with patients (n=20) and their caregivers (n=10) post-study will also be conducted to gain insight into their experience with the application.

Read the detailed description

By 2030, prostate cancer will be the most commonly diagnosed cancer in North America. To mitigate this impending challenge, comprehensive support mechanisms for disease and treatment-specific changes in health and wellbeing must be proactively designed and thoughtfully implemented for streamlined survivorship care. Mobile health applications have been lauded as a promising complement to current outpatient treatment and monitoring strategies, but have not yet been widely used to support prostate cancer survivorship needs. A realist evaluation is needed to examine the impact of such applications on the prostate cancer survivorship experience.

The investigators seek to gain an understanding of how a mobile health application for prostate cancer survivorship care called Ned ("No Evident Disease") is adopted and accepted by patients, caregivers and clinicians. The investigators also aim to determine the effect of Ned on health-related quality of life, satisfaction with cancer care, unmet needs, self-efficacy, and prostate cancer-related levels of anxiety.

The Ned case study is a 12-month mixed methods embedded single-case study with a nested within-group pre-post comparison of health outcomes. 400 patients, 200 caregivers, and 10 clinicians will be given access to Ned. Participants will be asked to complete study assessments at baseline, 2 months, 6 months and 12 months. 30 semi-structured qualitative interviews will be conducted with patients (n=20) and their caregivers (n=10) post-study to gain insight into their experience with the application.

This will be the first realist case study to evaluate an application for prostate cancer survivorship care. Prostate cancer survivors are set to increase in number and longevity, heightening the need for integrated survivorship solutions to provide them with optimal and durable outcomes. The knowledge gained from this study will comprehensively inform how and why Ned works, for whom, and in what circumstances. Understanding the impact of digital health interventions like Ned on how survivors care for themselves is critical to realising patient-centered care.

02

Conditions studied

  • Prostate Cancer

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Keywords

  • prostate-specific antigen
  • prostate cancer survivorship
  • mobile health
  • realist evaluation
  • case study
03

In context

Prostatic Neoplasms

6,370 studies on the registry are indexed under Prostatic Neoplasms; 1,400 are open to participants now.

This study's planned enrollment of 610 is above the median of 58 across 4,822 interventional studies indexed under Prostatic Neoplasms.

Browse Prostatic Neoplasms studies →

Lead sponsor

This is the only study on the registry with Centre for Global eHealth Innovation as lead sponsor.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
Male
Accepts healthy volunteers
No

Eligibility criteria

Patients must meet the following eligibility criteria to be enrolled into the study:

  • 18 years of age or older
  • Receiving care at the THP Mississauga Hospital or Credit Valley Hospital
  • Pathology report confirming prostate cancer diagnosis via transrectal, transperineal or transurethral biopsy (standard 12-core template)
  • Life expectancy > 1 year
  • No concomitant cancer diagnosis
  • Own a device that is compatible with the Ned application and is web-enabled through a data plan and/or wifi capabilities (e.g. laptop, desktop, tablet, smartphone)
  • Able to read, write and speak English
05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
610 participants (estimated)

Study arms

  • Experimental
    Ned Group

    Participants in the Ned case study (patients, caregivers, clinicians) will receive access to the Ned application. Ned ("No Evident Disease") is the first application to provide patients with access to individual-level prostate-specific antigen values streamed directly from the Ontario Laboratory Information System to their own smartphone. The application aims to promote self-care by informing patients directly of their PSA results and providing them with a personalised view of their own symptoms. It supports real-time clinical decision-making by providing clinicians with patient-reported outcomes collected in-app, and includes a curated educational feed and support group links.

    Behavioral: Ned

Interventions

  • BehavioralNed

    Prostate cancer survivorship application.

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What researchers measure

Primary outcomes

  1. Adoption

    The number of patients, caregivers and clinicians who are invited to open a Ned account, and the consequent number of Ned accounts created; measured using analytics log data.

    Time frame: Continuous throughout 12 month study duration

  2. Acceptability

    The perception of Ned as an acceptable addition to the standard of care; measured using (i) analytics log data (ii) validated questionnaires (iii) semi-structured interviews.

    Time frame: Continuous throughout 12 month study duration

Secondary outcomes

  1. Health-related quality of life

    Health-related quality of life will be measured using a validated questionnaire. Data will be collected at baseline, 2 months, 6 months, and 12 months.

    Time frame: 12 month study duration

  2. Satisfaction with cancer care

    Satisfaction with cancer care will be measured using a validated questionnaire. Data will be collected at baseline, 2 months, 6 months, and 12 months.

    Time frame: 12 month study duration

  3. Unmet needs

    Unmet needs will be measured using a validated questionnaire. Data will be collected at baseline, 2 months, 6 months, and 12 months.

    Time frame: 12 month study duration

  4. Self-efficacy

    Self-efficacy will be measured using a validated questionnaire. Data will be collected at baseline, 2 months, 6 months, and 12 months.

    Time frame: 12 month study duration

  5. Prostate cancer-related levels of anxiety

    Prostate cancer-related levels of anxiety will be measured using a validated questionnaire. Data will be collected at baseline, 2 months, 6 months, and 12 months.

    Time frame: 12 month study duration

07

Study locations

1 of 1 sites recruiting
  • Centre for Global eHealth Innovation
    Toronto, Ontario M5G 2C4, Canada
    • Quynh Pham, MSc · Contact · qpham@ehealthinnovation.org · 1-647-667-2573
    • Andrew Feifer, MD, MPH · Principal investigator
    • Joseph A. Cafazzo, PhD, PEng · Sub investigator
    • Quynh Pham, MSc · Sub investigator
    Recruiting
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References and documents

Related links

Individual participant data

Plan to share: No

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 12, 2017, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT03207113
Lead sponsor
Centre for Global eHealth Innovation
Collaborators
Trillium Health Partners, University Health Network, Toronto
Responsible party
Sponsor
First posted
Jul 2, 2017
Start date
Oct 2017 (estimated)
Primary completion
Mar 2018 (estimated)
Completion
Mar 2019 (estimated)
Last update
Oct 12, 2017

Study contacts

Quynh Pham, MSc
Contact
qpham@ehealthinnovation.org
1-647-667-2573
Andrew Feifer, MD, MPH
principal investigator · Trillium Health Partners

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Oct 2017. You cannot join it, but the record below documents what was studied.

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