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N/A Completed N=65

Feasibility Study of the Head and Neck Survivorship Tool: Assessment and Recommendations (HN-STAR)

Source: ClinicalTrials.gov NCT02571673 ↗
Enrolled (actual)
65
Serious AEs
0.0%
Results posted
Apr 2024
Primary outcomePrimary: Recommendations for Cancer Surveillance (Patient-reported Outcomes From the Survivor Self-Assessment) — 93 % of pts w/accurate TS for primary site

Summary

This study is being done to understand how survivors of head and neck cancer think they can make HN-STAR (the Survivor Self-Assessment, the survivorship clinic experience, and the Survivorship Care Plan the best it can be. Once the investigators have your input and input from other survivors, they can make changes to HN-STAR, so that they can test this tool in a larger study. The larger study will tell them whether using HN-STAR improves the care of head and neck cancer survivors.

Outcome Measures

OutcomeResultp-value
PRIMARY
Recommendations for Cancer Surveillance (Patient-reported Outcomes From the Survivor Self-Assessment)
93

Eligibility Criteria

Inclusion Criteria

Aim 1: Part 1

  • Have completed treatment for head and neck cancer at least 1 year prior to survivorship visit and have no evidence of disease
  • Have a primary care provider
  • Be able to provide informed consent
  • Be able to speak and read English
  • Be at least 18 years old

Aim 1: Part 2

  • Have completed treatment for head and neck cancer at least 1 year prior to survivorship visit and have no evidence of disease
  • Have a primary care provider
  • Be able to provide informed consent
  • Be able to speak and read English
  • Be at least 18 years old

Exclusion Criteria

Aim 1: Parts 1 and 2 is the same

  • Patients or providers who cannot speak or read English
  • Patients with cognitive, visual, or motor impairment such that they cannot complete the Survivor Self-Assessment as assessed by the research team.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02571673). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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