ACOS: AIMS Cancer Outcomes Study

Sponsor
Advanced Integrative Medical Science Institute (Other)
Overall Status
Recruiting
CT.gov ID
NCT04495790
Collaborator
(none)
500
1
127.4
3.9

Study Details

Study Description

Brief Summary

The overall aim is to describe disease-free survival (DFS) in early stage cancer patients and three-year overall survival (OS) outcomes in advanced stage cancer patients receiving Advanced Integrative Oncology (AIO) treatment in a prospective consecutive case series outcomes study. We will collect data and study outcomes for patients with cancer who receive care at AIMS Institute.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    It is estimated that between 50 and 80% of cancer patients in the United States (US) supplement their conventional medical treatment regimen with some form of complementary or alternative medicine (CAM) therapy or practice. A smaller percentage of these patients receive medical treatment from naturopathic doctors (NDs) who are board certified in naturopathic oncology (Fellows of the American Board of Naturopathic Oncology, FABNO) or have equivalent experience in caring for cancer patients. This level of care is being defined here as Advanced Integrative Oncology (AIO). AIO clinics provide comprehensive science- and experience-based naturopathic medical oncology integrated with the individual patient's conventional medical treatment.

    Although there have been some studies of alternative and complementary medicine use by both adult and pediatric cancer patients, little is known about the effectiveness of naturopathic medicine provided to patients with cancer in an integrative setting. Increasing numbers of parents of children seek out naturopathic physicians and other integrative oncologists for evidence-based complementary integrative therapy that is coordinated with the child's standard oncology treatment plan. The AIMS Institute provides nutritional and botanical medicine care to children with leukemia, brain cancer, and osteosarcoma. Despite the widespread use of integrative oncology by children with cancer, little is known about the effectiveness of these therapies in pediatric cancer patients.

    While there is scientific evidence supporting specific treatments that are commonly used, systematic study of their effectiveness, especially when used in combination as commonly recommended, is sparse. We believe that an early step in the evaluation of clinical outcomes associated with CAM is to take a health services approach and seek to answer the question: "Does exposure to AIO services improve the clinical outcomes of patients with cancer?"

    Study Design

    Study Type:
    Observational [Patient Registry]
    Anticipated Enrollment :
    500 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Advanced Integrative Oncology Treatment for Adult and Pediatric Patients With Cancer: A Prospective Outcomes Study
    Actual Study Start Date :
    May 18, 2020
    Anticipated Primary Completion Date :
    May 18, 2025
    Anticipated Study Completion Date :
    Dec 31, 2030

    Outcome Measures

    Primary Outcome Measures

    1. AIM 1 (survival) [5 Years]

      Measure DFS and OS in advanced stage cancer patients who receive AIO treatments at AIMS Institute.

    Secondary Outcome Measures

    1. AIM 2 (treatment) [5 Years]

      Describe AIO treatments prescribed and provided by AIMS physician and their medical staff.

    2. AIM 3 (correlate survival with treatment) [5 Years]

      Correlate survival outcomes with treatments received.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    N/A and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    1. A new patient coming in for a first office call (FOC) or first consultation via telemedicine with a diagnosis of cancer, or

    2. An established patient with a diagnosis of cancer receiving treatment at the AIMS Institute;

    3. If over 18 years of age are able to understand study design adequately and provide signed informed consent (IC) to enrollment;

    4. If younger than 18 years of age informed assent from the child and informed consent from a parent or guardian who is able to understand the study design adequately and provide signed informed consent for the pediatric patient;

    5. A confirmed diagnosis of cancer based on medical oncology medical records.

    Exclusion Criteria:
    1. Patients not diagnosed with cancer;

    2. Telehealth patients;

    3. Cannot read or understand English well enough to read and sign the consent form and complete the questionnaires;

    4. Unwilling to participate in the AIMS Institute observational study.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 AIMS Institute Seattle Washington United States 98102

    Sponsors and Collaborators

    • Advanced Integrative Medical Science Institute

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Advanced Integrative Medical Science Institute
    ClinicalTrials.gov Identifier:
    NCT04495790
    Other Study ID Numbers:
    • ACOS
    First Posted:
    Aug 3, 2020
    Last Update Posted:
    Aug 4, 2020
    Last Verified:
    Aug 1, 2020
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Advanced Integrative Medical Science Institute
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Aug 4, 2020