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Completed

NCT Number: NCT03951090

Geriatric Assessment Reporting in Real Time (GARRT) in Non-electively Hospitalized Older Cancer Patients

This study prospectively evaluates the impact of geriatric assessment reporting in real-time (GARRT) on key hospital based outcomes in a cohort of non-electively hospitalized older (> 70 years) adults with cancer.

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Key information

Conditions

Age range

70 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

UNC Lineberger Comprehensive Cancer Center

Chapel Hill, North Carolina, 27599, United States

About this study

This study evaluates the impact of geriatric assessment reporting in real-time (GARRT) on key hospital based outcomes in non-electively hospitalized older (> 70 years) adults with cancer. Participants will be randomly assigned to the GARRT group, or the control group. All participants will fill out user friendly questionnaire called the geriatric assessment. The results of the geriatric assessment will be given to the physicians of participants in the GARRT group in real-time. The physicians of participants in the control group will not receive real time results.

This study will compare the referral rates of participants in each group to determine if providing real-time results of the geriatric assessment impact referral rates.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Age 70 years or older.
  • English speaking.
  • Admitted to UNC Hospitals non-electively within 72 hours.
  • Biopsy proven solid tumor or myeloma or lymphoma.
  • Newly diagnosed cancer patients for whom active cancer directed therapy is planned within the next six months or patients on active cancer directed therapy either currently or within the previous 6 months.
  • Signed written IRB-approved informed consent.

Exclusion criteria

  • Patients meeting any of the following exclusion criteria at baseline will be excluded from study participation. Patients with a life expectancy <6 weeks
  • Patients who are <48 hours post-surgery.
  • Patients who are admitted to an intensive care setting.
  • Patients with acute myeloma lymphoma (AML) or other high grade hematologic malignancies.
  • Patients undergoing bone marrow transplant or admitted to the bone marrow transplant unit.

Treatment and study plan

Results of the brief geriatric assessment

Other

Providers will receive results of the brief geriatric assessment with recommendations for address deficits identified through the results of the brief geriatric assessment

No results of brief geriatric assessments

Other

Providers will not receive results of the brief geriatric assessment. Participants will receive standard of care treatment

Primary outcomes

  1. Referral rate for GA-identified deficits in intervention and control groups

    Time frame: 2 years

    Number of participants with at least one referral for a GA-idenfied deficit

Secondary outcomes

  1. Referral to Physical and Occupational therapy

    Time frame: 2 years

    Number of times physical and occupation therapy referral was given in Intervention and Control group

  2. Referral to Geriatic Consultation

    Time frame: 2 years

    Number of times a Geriatric Consultation referral was given in Intervention and Control group

  3. Referral to Clinical Pharmacist

    Time frame: 2 years

    Number of times Clinical Pharmacist referral was given in Intervention and Control group

  4. Referral to Nutritionist

    Time frame: 2 years

    Number of times Nutritionist referral was given in Intervention and Control group

  5. Referral to psyhcosocial support team

    Time frame: 2 years

    Number of times psychosocial support referral was given in Intervention and Control group

  6. Physician Reported New information

    Time frame: 2 years

    Number of times physicians answer "yes" to the questions "did report provide new information about patient deficits that would warrant a referral"

  7. Physician Reported Satisfaction

    Time frame: 2 years

    Number of times physician indicate "yes" report was helpful when asked "Is this report useful"

Sponsors and collaborators

Lead sponsor

UNC Lineberger Comprehensive Cancer Center

Other

Registry information

Important dates

Study start
2016
Primary completion
2018
Study completion
2018
First posted
May 15, 2019
Registry last updated
May 15, 2019

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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