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Assessment, GeriatricNCT00977834

Assessment of Older Adults With Cancer: Feasibility of Computer Survey Methodology

An observational study of Assessment, Geriatric, run by City of Hope Medical Center at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record

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Trial summary

The purpose of this study is to evaluate the possibility of using a computer-based survey to gather information from older patients and their caregivers about the patient's daily activities, need for assistance, other medical problems, mood, nutrition and symptoms. Read more about this study

Who is it for?
Ages 65 years and olderHealthy volunteers can take part
Conditions the study is for
Assessment, Geriatric
How many people
200 participants
Where
1 siteUnited States
Study dates
3 Aug 2009to 26 Jul 2011
Phase
Observational

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 65 years and older
  • All sexes
  • Healthy volunteers accepted
  • Older adult

Study population: Brawerman Center-Outpatient Clinics (City of Hope)

Who may be able to join

  • Patients must be > age of 65
  • Diagnosis of lymphoma or lung cancer
  • Be able to provide informed consent

Who cannot join

  • Not fluent in English (because not all questionnaires have been validated in other languages)

Trial locations and contacts

1 site in 1 country.

United States1 site
  • City of Hope Medical Center

    Duarte, California, 91010

Other trials in United States

About this study

The purpose of this study is to evaluate the possibility of using a computer-based survey to gather information from older patients and their caregivers about the patient's daily activities, need for assistance, other medical problems, mood, nutrition and symptoms. Researchers will evaluate how many subjects are able to complete the survey on their own and the length of time needed to do so. Also, researchers will analyze the types of responses to each item and whether subjects are satisfied with the questionnaire.

Read the detailed description

Patients older than age 65, in comparison to those younger than 65, have an 11-fold increased cancer incidence and a 16-fold increase in cancer mortality. The population at risk is growing rapidly: the number of adults age 65 and older is expected to double in the next 30 years. In order to adequately care for this growing population of older adults, oncologists need an assessment tool that provides information regarding an older individual's "functional age" in comparison to their "chronological age." The technology of geriatric assessment could potentially help identify those older adults who are more vulnerable to complications from cancer treatment. This inter-disciplinary assessment provides information regarding the patient's functional status, comorbid medical conditions, other medications, nutritional status, psychological state, social support, and cognition.

Hurria and colleagues developed a geriatric assessment for older adults with cancer, which includes well validated measures of functional status, comorbid medical conditions, nutritional status, psychological state, cognitive function, social activity, and social support. Pilot data demonstrates the feasibility of this assessment which can be completed in less than 30 minutes; however, this assessment is completed by "pencil and paper" and requires an interviewer to deliver and score the assessment.

Loscalzo, Clark, and colleagues have developed a computer methodology in order to assess the needs of patients with cancer of all ages. The assessment is completed by the patients and a scoring algorithm is developed to provide a summary of the patient's needs for the healthcare team. This assessment is highly successful at identifying the needs of patients of all ages.

In this protocol, we will merge the research interests of Hurria, Loscalzo, and Clark by developing a computer survey program to capture the physical and psychological needs of older adults with cancer. The goal of this study is to evaluate the feasibility of computer survey methodology among older adults with cancer. For the purposes of this protocol we will accrue patients with lymphoma and lung cancer.

Schema:

  1. Identify an older adult (age 65 and older) with lymphoma or lung cancer.
  2. Describe the study to the patient: patient consents or refuses.
  3. Consenting patients complete the geriatric assessment via a computer survey.
  4. The following feasibility data will be captured: length of time to complete the assessment, patient's need for assistance to complete the assessment, satisfaction with the use of computer survey methodology to complete the assessment.
  5. The primary caretaker (if available) will be invited to participate in the protocol and complete a caregiver's survey of the patient's needs and questions about caregiver burden.
Keywords
Geriatric Assessment

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT00977834
Study groupRoleWhat they receive
Group 1Patients with lymphoma or lung cancer
Group 2Caregivers

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Feasibility of delivering the geriatric assessment via computer survey methodology.

    Measured: Upon enrollment (one timepoint)

Secondary outcomes (1)
  1. % of patients who do not enter the study and reason why

    Measured: Upon enrollment (one timepoint)

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted16 Sep 2009 (estimated)
  2. Study start3 Aug 2009
  3. Primary completion26 Jul 2011
  4. Study completion26 Jul 2011

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Cross-sectional
Enrolment
200 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT00977834
Sponsor's protocol ID
08147
Other IDs
P50CA107399-04, K23AG026749-01
Status last verified
Oct 2026
First submitted
15 Sep 2009
Last updated
22 Oct 2026
Results posted
No
Data monitoring committee
Yes

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