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OpenTrials
Completed

NCT Number: NCT00970125

Using Video Images to Improve Advance Care Planning in Patients With Cancer

The purpose of this study is to study whether preferences for the goals of care for 80 subjects with end-stage cancer are altered after viewing a video outlining the goals of care compared to their initial preferences after hearing a verbal description of the goals of care alone.

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Key information

Age range

21 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Memorial Sloan Kettering

New York, 10065, United States

About this study

The purpose of this study is to study whether preferences for the goals of care for 80 subjects with end-stage cancer are altered after viewing a video outlining the goals of care compared to their initial preferences after hearing a verbal description of the goals of care alone. Subjects will choose among three goals of care, life prolonging care, basic medical care, and comfort care.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Terminal, progressive cancer with poor prognosis whose treatment intent is palliative, based on the following definition:
  • All patients with brain cancer, liver cancer, inoperable non-small cell lung carcinoma, pancreatic cancer, or gallbladder cancer; OR
  • Patients with the following cancers: metastatic colon cancer or stage III or IV non-small cell lung cancer; OR
  • Patients with the following cancers, if first-line therapy has failed and limited response is expected to second-line therapy: breast cancer, colorectal cancer, head and neck cancer, stomach cancer, esophageal cancer, melanoma, leukemia, ovarian cancer, prostate cancer, renal cancer, sarcoma, lung cancer, myeloma, or lymphoma.
  • The terms terminal, progressive, poor prognosis, palliative intent and limited response will be judged by the patient's oncologist (and not by the RSA or consenting professional).
  • Return patient visit (defined as a patient known to the oncologist from previous assessments and treatments, where the working and personal relationship has been established and not a new patient to the clinic).
  • English speaking. Only English-speaking patients will be included in our present study since English is the validated language of our study tools.
  • Given the sensitive nature of the study, clinicians will decide whether the patient is a potentially appropriate subject based on their knowledge of the patient.
  • Able to provide informed consent.
  • Age greater than or equal to 21.

Exclusion criteria

  • MMSE < 25.
  • Psychological state not appropriate for end-of-life discussion as determined by the treating clinician.

Treatment and study plan

Video

Behavioral

outline of the goals of care

Primary outcomes

  1. end of life preference at time of interview

    Time frame: 5 minutes after survey

Secondary outcomes

  1. knowledge

    Time frame: 5 minutes after survey

  2. decisional conflict

    Time frame: 5 minutes after survey

Sponsors and collaborators

Lead sponsor

Massachusetts General Hospital

Other

Registry information

Important dates

Study start
2009
Primary completion
2011
Study completion
2011
First posted
Sep 2, 2009
Registry last updated
May 1, 2012

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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