Study to Determine Whether Cancer Symptom Control can be Enhanced Using Electronic Health Records


About this study

The purpose of this study is to determine whether control of moderate or worse sleep disturbance, pain, anxiety, depression, and fatigue among cancer survivors and patients with cancer will improve quality of life, symptom severity, function, and adherence to cancer treatment, and reduced health care utilization.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Please contact the study team to discuss whether or not you are eligible to participate in a study.

Inclusion Criteria:


  • Adults ≥ 18 years old.
  • Being seen for a solid or liquid cancer at a Midwest Mayo Clinic MCHS site or for a solid tumor at Mayo Clinic Rochester.

Exclusion Criteria:

  • Adults < 18 years old.
  • Lack of English Fluency.
  • Membership in a vulnerable population (prisoner, mentally handicapped, Axis I psychiatric condition).



Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status Contact

Rochester, Minn.

Mayo Clinic principal investigator

Andrea Cheville, M.D.

Contact us for the latest status

Contact information:

Andrea Cheville M.D.


More information


Publications are currently not available

Study Results Summary

Not yet available

Supplemental Study Information

Not yet available


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