Improving Decision-Making Encounters in Lung Cancer (iDECIDE) II: A Randomized Controlled Trial of a Low-Literacy Conversation Tool

Sponsor
OHSU Knight Cancer Institute (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05407168
Collaborator
Oregon Health and Science University (Other), American Cancer Society, Inc. (Other)
300
2
2
64.5
150
2.3

Study Details

Study Description

Brief Summary

This clinical trial evaluates the effectiveness of a conversation tool on patient-centered health and decision-making outcomes in patients with lung cancer making treatment decisions. This research is being conducted to help doctors understand the information patients need to participate in shared decision-making about their lung cancer treatment options. The focus of this research is to study how patients choose lung cancer treatment options and the information needed to make that choice, with a focus on patients with lower health literacy.

Condition or Disease Intervention/Treatment Phase
  • Other: Best Practice
  • Other: Health Promotion and Education
  • Other: Questionnaire Administration
N/A

Detailed Description

PRIMARY OBJECTIVES:
  1. Conduct a randomized, controlled trial evaluating the efficacy of a conversation tool on patient-centered health and decision-making outcomes among patients making lung cancer treatment decisions. A subset of participants from control and intervention groups will also have their clinic conversations with providers recorded II. Conduct in-depth, semi-structured qualitative audio or video recorded interviews among a subset of Aim 1 participants.

OUTLINE: Patients are randomized to 1 of 2 groups.

GROUP I: Patients review decision aid.

GROUP II: Patients receive standard of care.

After completion of study intervention, patients are followed up at 2 weeks, 3 months, and 6 months.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
300 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Investigator)
Primary Purpose:
Health Services Research
Official Title:
Improving Decision-Making Encounters in Lung Cancer (iDECIDE) II: A Randomized Controlled Trial of a Low-Literacy Conversation Tool
Anticipated Study Start Date :
Aug 15, 2022
Anticipated Primary Completion Date :
Sep 30, 2026
Anticipated Study Completion Date :
Dec 31, 2027

Arms and Interventions

Arm Intervention/Treatment
Experimental: Group I (decision aid)

Patients review decision aid.

Other: Health Promotion and Education
View decision aid

Other: Questionnaire Administration
Ancillary studies

Active Comparator: Group II (standard of care)

Patients receive standard of care.

Other: Best Practice
Receive standard of care
Other Names:
  • standard of care
  • standard therapy
  • Other: Questionnaire Administration
    Ancillary studies

    Outcome Measures

    Primary Outcome Measures

    1. Decision Satisfaction [Up to 6 months]

      Will be assessed using two scales: 1) The Decisional Conflict Scale, which contains 16 items. Higher scores indicate higher decisional conflict. 2) The Decisional Self-Efficacy Scale, which contains 11 items. Higher scores indicate higher self-efficacy.

    2. Efficacy of a conversation tool on patients' knowledge of lung cancer [Up 6 months]

      Will be assessed using nine questions from previously validated measures.

    3. Satisfaction with Communication/Confidence in Decision [Up to 6 months]

      Will be assessed using the 20-item COMRADE scale. Higher scores indicate better outcomes.

    Secondary Outcome Measures

    1. Quality of Life [Up to 6 months.]

      Will be assessed by the Functional Assessment of Cancer Therapy -- Lung scale. This scale has 27 items. Higher scores indicate higher quality of life.

    2. Depression/Anxiety [Up to 6 months]

      Will be assessed using the 4 item Patient Health Questionnaire for Anxiety and Depression scale. Scores greater than or equal to 3 on the first two questions suggest anxiety, and scores greater than or equal to 3 on the last two questions suggest depression.

    3. Participation in Decision-Making [Up to 6 months]

      Will be assessed using the 2-item Control Preferences Scale. Answers of 1 or 2 on both items are categorized as "patient controlled", answers of 3 are categorized as "shared", and answers of 4 or 5 are categorized as "physician-controlled."

    4. Patient-Reported Shared Decision-Making [Up to 6 months]

      Will be assessed using the 9-item Shared Decision-Making Questionnaire. Higher scores indicate higher shared decision-making.

    5. Decision Regret [Up to 6 months]

      Will be assessed using the 5-item Decision Regret Scale. Higher scores indicate high regret.

    6. Quality of Communication [Up to 6 months]

      Will be assessed using the ~30 item Patient Assessment of cancer Communication Experiences scale. Higher scores indicate higher perceived quality of communication.

    7. Shared-Decision Making [Up to 6 months]

      Will be assessed using the 12-item OPTION scale. Higher scores indicate higher quality shared-decision making.

    8. Number of Palliative Care Referrals [Up to 6 months]

      Will be assessed by conducting chart review

    9. Treatment Decision-Making Concordance [Up to 6 months]

      Will be assessed by observing the treatment received and the treatment most aligned with responses to the conversation tool. If the treatment received is the same treatment the patient preferred according to the conversation tool, the treatment decision will be considered concordant.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 99 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • AIM 1: Suspected lung cancer

    • AIM 1: English fluency

    • AIM 1: > 6-month life expectancy

    • AIM 1: Score of > 3 on the cognitive impairment screener

    • AIM 2 PARTICIPANTS: Participation in Aim 1

    • AIM 2 CLINICIANS: Discussing lung cancer treatment decisions with Aim 1 participants

    • VA-SPECIFIC REQUIREMENT (inclusion of non-Veterans): Non-Veterans will be recruited for this study. Non-Veterans are an important component to this project since they will provide outside perspective. In this way, results of this study will be more generalizable

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 OHSU Knight Cancer Institute Portland Oregon United States 97239
    2 Portland VA Medical Center Portland Oregon United States 97239

    Sponsors and Collaborators

    • OHSU Knight Cancer Institute
    • Oregon Health and Science University
    • American Cancer Society, Inc.

    Investigators

    • Principal Investigator: Donald R Sullivan, MD, MA, MCR, OHSU Knight Cancer Institute

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Donald R Sullivan, MD, MA, MCR, Principal Investigator, OHSU Knight Cancer Institute
    ClinicalTrials.gov Identifier:
    NCT05407168
    Other Study ID Numbers:
    • STUDY00023160
    • NCI-2021-09819
    • STUDY00023160
    First Posted:
    Jun 7, 2022
    Last Update Posted:
    Aug 11, 2022
    Last Verified:
    Aug 1, 2022
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Aug 11, 2022