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PROMs To Improve Care- Standardized vs Patient Specific

Primary Purpose

Hand Injuries

Status
Withdrawn
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Patient Specific Functional Scale
PROMIS PF
Sponsored by
Stanford University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Hand Injuries

Eligibility Criteria

18 Months - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • hand surgery patients over age 18, english fluency and literacy, able to take informed consent

Exclusion Criteria:

-

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Active Comparator

    Experimental

    Arm Label

    PSFS group

    PROMIS PF group

    Arm Description

    Patients in this arm will complete the patient specific functional scale (PSFS) during their visits

    Patients in this arm will complete the PROMIS Physical Function during their visits

    Outcomes

    Primary Outcome Measures

    Decisional Conflict Scale (DCS)
    DCS is a validated tool that measures patient uncertainty about decisions. it is scored 0 to 100, with higher scores indicating greater conflict about the decisions.

    Secondary Outcome Measures

    Full Information

    First Posted
    July 18, 2019
    Last Updated
    August 6, 2021
    Sponsor
    Stanford University
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    1. Study Identification

    Unique Protocol Identification Number
    NCT04027569
    Brief Title
    PROMs To Improve Care- Standardized vs Patient Specific
    Official Title
    PROMs To Improve Care: A Pragmatic RCT on Standardized and Patient Specific PROMs on Outcomes After Hand Surgery
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    August 2021
    Overall Recruitment Status
    Withdrawn
    Why Stopped
    Logistics (Research Staffing)
    Study Start Date
    November 2021 (Anticipated)
    Primary Completion Date
    December 2021 (Anticipated)
    Study Completion Date
    December 2021 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Stanford University

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    To examine the impact of using 2 validated PROMs during the care of an orthopaedic condition on shared decision making, patient centered care, and patient outcomes.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Hand Injuries

    7. Study Design

    Primary Purpose
    Health Services Research
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    0 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    PSFS group
    Arm Type
    Active Comparator
    Arm Description
    Patients in this arm will complete the patient specific functional scale (PSFS) during their visits
    Arm Title
    PROMIS PF group
    Arm Type
    Experimental
    Arm Description
    Patients in this arm will complete the PROMIS Physical Function during their visits
    Intervention Type
    Other
    Intervention Name(s)
    Patient Specific Functional Scale
    Intervention Description
    A validated patient reported outcome measure that asks patients to write down activities and score them 0 to 10.
    Intervention Type
    Other
    Intervention Name(s)
    PROMIS PF
    Intervention Description
    A computer adaptive, validated patient reported outcome measure that measures physical function on a 1 to 100.
    Primary Outcome Measure Information:
    Title
    Decisional Conflict Scale (DCS)
    Description
    DCS is a validated tool that measures patient uncertainty about decisions. it is scored 0 to 100, with higher scores indicating greater conflict about the decisions.
    Time Frame
    Immediately after the clinical encounter, same day as clinical encounter

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Months
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: hand surgery patients over age 18, english fluency and literacy, able to take informed consent Exclusion Criteria: -
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Robin N Kamal, MD MBA
    Organizational Affiliation
    Stanford University
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No
    IPD Sharing Plan Description
    There is no plan to share IPD

    Learn more about this trial

    PROMs To Improve Care- Standardized vs Patient Specific

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