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Impact of Treatment Consultation Recordings on Cancer Patient Outcomes: A Prospective, Parallel, Randomized Controlled Trial


N/A
18 Years
N/A
Not Enrolling
Both
Brain Tumor, Neuroendocrine Cancer

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Trial Information

Impact of Treatment Consultation Recordings on Cancer Patient Outcomes: A Prospective, Parallel, Randomized Controlled Trial


Inclusion Criteria:



- presenting with a primary diagnosis of non-recurrent or metastatic brain, or
neuroendocrine cancer

- 18 years of age or older

- able to read and communicate using the English language

- access to a computer to enable consultation playback

Exclusion Criteria:

- deemed by a treating clinician (or primary nurse for the treating clinician) to have
any severe psychiatric condition or cognitive dysfunction that precludes provision of
free and informed consent to participate

Type of Study:

Interventional

Study Design:

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Supportive Care

Outcome Measure:

Change from Baseline in Control Preferences Scale at 1-week post-consultation

Outcome Description:

Subjective report of actual role played in decision making.

Outcome Time Frame:

1-week post-consultation

Safety Issue:

No

Principal Investigator

Thomas F Hack, PhD

Investigator Role:

Principal Investigator

Investigator Affiliation:

University of Manitoba

Authority:

Canada: Research Ethics Board

Study ID:

H2013:085

NCT ID:

NCT01866228

Start Date:

June 2013

Completion Date:

December 2015

Related Keywords:

  • Brain Tumor
  • Neuroendocrine Cancer
  • Consultation Recording
  • Brain Tumor
  • Neuroendocrine Cancer
  • Quality of Life
  • Patient Satisfaction
  • Brain Neoplasms

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