Skip to content

The Effects of Aggressive Patient Management on Cancer Therapy Management

The Effects of Aggressive Patient Management on Cancer Therapy Management

Status
Withdrawn
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00962572
Enrollment
0
Registered
2009-08-20
Start date
2009-01-31
Completion date
2010-12-31
Last updated
2012-04-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cancer

Keywords

Outcomes, Cancer, Radiotherapy, Socio-economic

Brief summary

A study to see if coordinated aggressive patient management will improve patient treatment outcomes and is cost effective.

Detailed description

This is an observational study of the effects of aggressive patient management. The records of 50 patients treated under the aggressive management plan will be matched with the records of 50 previous patients and attempts made to assess the improvement, if any, found. Statistical analysis will compare the outcomes of the study group and the matched control group for initial completion of planned therapy as per prescription, weight loss during therapy, intercurrent illness, and intercurrent hospitalizations. Long term analysis will compare the study group's outcomes (compared to expected outcomes) compared to the matched control group.

Interventions

BEHAVIORALPatient management

Aggressive patient management will be implemented by a corps of patient manager volunteers backed by a transportation, nutrition, and social services network. The social services professionals will work with the volunteers to establish the support needed for each patient. The volunteer managers will in turn constantly monitor that such support is addressing the patient's ability to be treated. Access to sponsored housing will be coordinated. Nutritional support will be coordinated by the Dietary department and will consist of counseling, and supplements when necessary. Provision of supplemental feeding for housed patients will be arranged.

Sponsors

University of Mississippi Medical Center
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* live 45 minutes from treatment facility * family income less than 200% federal poverty guideline

Exclusion criteria

* none

Design outcomes

Primary

MeasureTime frame
To test effects of intensive patient management on patient's compliance with referral and subsequent treatment protocol.1 year

Secondary

MeasureTime frame
To test if increased compliance results in better therapy outcomes and fewer complications of the disease process as evidenced by increased survival and fewer intercurrent hospitalizations.1 year

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026