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Communication Effectiveness in Cancer Treatment

Wake Forest University (WFU) logo

Wake Forest University (WFU)

Status

Completed

Conditions

Malignant Neoplasm

Treatments

Other: medical chart review
Other: questionnaire administration

Study type

Observational

Funder types

Other
NIH

Identifiers

NCT02197091
P30CA012197 (U.S. NIH Grant/Contract)
IRB00028889
NCI-2014-01478 (Registry Identifier)
CCCWFU #99514 (Other Identifier)

Details and patient eligibility

About

This pilot research trial studies communication effectiveness in cancer treatment. Studying how well patients and their doctors communicate about the treatment being given for cancer may help improve the decisions that patients and physicians make together.

Full description

PRIMARY OBJECTIVES:

I. To assess the feasibility of measuring discrepancies between patient and physician perceptions about the intent of therapy.

SECONDARY OBJECTIVES:

I. To explore possible correlation between various patient satisfaction indicators and discrepant patient perceptions about their care.

II. To gather exploratory data on patient characteristics that might correlate with discrepant patient perceptions about their care.

OUTLINE:

Patients complete questionnaires, including the Functional Assessment of Cancer Therapy-Treatment Satisfaction (FACIT-TS-G), the Functional Assessment of Cancer Therapy-Spiritual Well Being (FACIT-Sp12), the Medical Outcomes Study Social Support Survey (MOS-SSS), and the Distress Thermometer (DT). Doctors also complete a questionnaire. Patients' medical records may be reviewed, if necessary.

After completion of study, patients are followed up for 5 years.

Enrollment

100 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  • Patients with a diagnosis of cancer
  • Patients must have been in active therapy for cancer for at least one month or have a scheduled surgical treatment of their cancer
  • Ability to understand and the willingness to sign an institutional review board (IRB)-approved informed consent document

Trial design

100 participants in 1 patient group

Observational (communication in oncology treatment)
Description:
Patients complete questionnaires, including the FACIT-TS-G, the FACIT-Sp12, the MOS-SSS, and the DT. Doctors also complete a questionnaire. Patients' medical records may be reviewed, if necessary.
Treatment:
Other: questionnaire administration
Other: medical chart review

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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