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ID

42132

Beschrijving

CALGB: Y-ME COUNSELOR TELEPHONE CONTACT FORM Comparison of Combination Chemotherapy Regimens in Treating Older Women Who Have Undergone Surgery for Breast Cancer Source Form: NCI FormBuilder: https://formbuilder.nci.nih.gov/FormBuilder/formDetailsAction.do?method=getFormDetails&formIdSeq=A50CF1AD-5DEE-3887-E034-080020C9C0E0

Link

https://formbuilder.nci.nih.gov/FormBuilder/formDetailsAction.do?method=getFormDetails&formIdSeq=A50CF1AD-5DEE-3887-E034-080020C9C0E0

Trefwoorden

  1. 12-12-14 12-12-14 - Martin Dugas
  2. 13-04-21 13-04-21 - Dr. rer. medic Philipp Neuhaus
Geüploaded op

13 april 2021

DOI

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Licentie

Creative Commons BY-NC 3.0 Legacy

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    Breast Cancer NCT00024102 Quality of Life - CALGB: Y-ME COUNSELOR TELEPHONE CONTACT FORM - 2044777v3.0

    INSTRUCTIONS: The Y-ME counselor will complete and submit this form as required by the protocol. Information in the upper right box muse be completed for this form to be accepted. For optimal accuracy use black ink. Mark an X in the appropriate box for fields with a choice. Print text in capital letters. Avoid contact with the edges of the boxes. Retain a copy for your records and send the original to the CALGB Data Management Center.

    General Information
    Beschrijving

    General Information

    Alias
    UMLS CUI-1
    C1508263
    CALGB Form
    Beschrijving

    CALGBForm

    Datatype

    text

    CALGB Form
    Beschrijving

    CALGBForm

    Datatype

    text

    Y-ME Patient ID (6.)
    Beschrijving

    Y-MEPatientID

    Datatype

    text

    Y-ME Patient ID (6.)
    Beschrijving

    Y-MEPatientID

    Datatype

    text

    Patient enrolled in 49907 (1.)
    Beschrijving

    Patientenrolledin49907

    Datatype

    text

    Alias
    NCI Thesaurus ValueDomain
    C25180
    UMLS 2011AA ValueDomain
    C1522602
    Counselor's Name (2.)
    Beschrijving

    Counselor'sName

    Datatype

    text

    Date of session (M)
    Beschrijving

    Dateofsession

    Datatype

    date

    Alias
    NCI Thesaurus ValueDomain
    C25164
    UMLS 2011AA ValueDomain
    C0011008
    Time session began ([hour/minute])
    Beschrijving

    Timesessionbegan

    Datatype

    text

    Time session ended ([hour/minute])
    Beschrijving

    Timesessionended

    Datatype

    text

    Session with (mark one with an X)
    Beschrijving

    Sessionwith

    Datatype

    text

    Topics Discussed (mark all that apply with an X)
    Beschrijving

    TopicsDiscussed

    Datatype

    text

    Patient asked the following about this clinical trial (mark all that apply with an X)
    Beschrijving

    Patientaskedthefollowingaboutthisclinicaltrial

    Datatype

    text

    Other, specify (patient asked about this clinical trial) (C.)
    Beschrijving

    Other,specify(patientaskedaboutthisclinicaltrial)

    Datatype

    text

    Consent Form (mark all that apply with an X)
    Beschrijving

    ConsentForm

    Datatype

    text

    Specific protocol-related issues (mark all that apply with an X)
    Beschrijving

    Specificprotocol-relatedissues

    Datatype

    text

    Other, specify (specific protocol-related issues) (E.)
    Beschrijving

    Other,specify(specificprotocol-relatedissues)

    Datatype

    text

    Other Topics Discussed, specify below
    Beschrijving

    OtherTopicsDiscussed,specifybelow

    Datatype

    text

    CALGB Form
    Beschrijving

    CALGBForm

    Datatype

    text

    CALGB Form
    Beschrijving

    CALGBForm

    Datatype

    text

    Y-ME Patient ID (6.)
    Beschrijving

    Y-MEPatientID

    Datatype

    text

    Y-ME Patient ID (6.)
    Beschrijving

    Y-MEPatientID

    Datatype

    text

    Telephone Interview
    Beschrijving

    Telephone Interview

    Alias
    UMLS CUI-1
    C0021823
    UMLS CUI-2
    What were the patient's concerns about participating in this clinical trial? (mark all that apply)
    Beschrijving

    Patient's concerns about participating in this clinical trial

    Datatype

    text

    Alias
    UMLS CUI-1
    C2699424
    UMLS CUI-2
    C0681850
    Other, specify (patient's concerns about participating in this clinical trial)
    Beschrijving

    Other, specify (patient's concerns about participating in this clinical trial)

    Datatype

    text

    Most Important (patient's concerns about participating in this trial)
    Beschrijving

    Most Important (patient's concerns about participating in this trial)

    Datatype

    text

    2nd Most Important (patient's concerns about participating in this trial)
    Beschrijving

    2nd Most Important (patient's concerns about participating in this trial)

    Datatype

    text

    3rd Most Important (patient's concerns about participating in this trial)
    Beschrijving

    3rd Most Important (patient's concerns about participating in this trial)

    Datatype

    text

    What was the outcome at the end of the call? (mark all that apply with an X)
    Beschrijving

    Whatwastheoutcomeattheendofthecall?

    Datatype

    text

    Sent some information brochures to the patient [specify which:]
    Beschrijving

    Sent some information brochures to the patient [specify which:]

    Datatype

    text

    Alias
    UMLS CUI-1
    C0030258
    Other, specify (outcome at the end of the call)
    Beschrijving

    Other,specify(outcomeattheendofthecall)

    Datatype

    text

    Completed By (Print or Type Name)
    Beschrijving

    CompletedBy

    Datatype

    text

    Date Completed
    Beschrijving

    Date Completed

    Datatype

    date

    Alias
    UMLS CUI-1
    C0011008

    Similar models

    INSTRUCTIONS: The Y-ME counselor will complete and submit this form as required by the protocol. Information in the upper right box muse be completed for this form to be accepted. For optimal accuracy use black ink. Mark an X in the appropriate box for fields with a choice. Print text in capital letters. Avoid contact with the edges of the boxes. Retain a copy for your records and send the original to the CALGB Data Management Center.

    Name
    Type
    Description | Question | Decode (Coded Value)
    Datatype
    Alias
    Item Group
    General Information
    C1508263 (UMLS CUI-1)
    CALGBForm
    Item
    CALGB Form
    text
    CALGBForm
    Item
    CALGB Form
    text
    Y-MEPatientID
    Item
    Y-ME Patient ID (6.)
    text
    Y-MEPatientID
    Item
    Y-ME Patient ID (6.)
    text
    Item
    Patient enrolled in 49907 (1.)
    text
    C25180 (NCI Thesaurus ValueDomain)
    C1522602 (UMLS 2011AA ValueDomain)
    Code List
    Patient enrolled in 49907 (1.)
    CL Item
    No (No)
    C49487 (NCI Thesaurus)
    C1298908 (UMLS 2011AA)
    CL Item
    Yes (Yes)
    C49488 (NCI Thesaurus)
    C1705108 (UMLS 2011AA)
    Counselor'sName
    Item
    Counselor's Name (2.)
    text
    Dateofsession
    Item
    Date of session (M)
    date
    C25164 (NCI Thesaurus ValueDomain)
    C0011008 (UMLS 2011AA ValueDomain)
    Timesessionbegan
    Item
    Time session began ([hour/minute])
    text
    Timesessionended
    Item
    Time session ended ([hour/minute])
    text
    Item
    Session with (mark one with an X)
    text
    Code List
    Session with (mark one with an X)
    CL Item
    Patient (Patient)
    C16960 (NCI Thesaurus)
    C0030705 (UMLS 2011AA)
    CL Item
    Family Member Or Friend (Family member or friend)
    Item
    Topics Discussed (mark all that apply with an X)
    text
    Code List
    Topics Discussed (mark all that apply with an X)
    CL Item
    Patient Asked The Following About This Clinical Trial (Patient asked the following about this clinical trial)
    CL Item
    Described Experience Of Being On A Clinical Trial/research Study: How It Differs From Just Being Treated 'off-protocol' (Described experience of being on a clinical trial/research study: How it differs from just being treated 'off-protocol')
    CL Item
    Consent Form (Consent Form)
    C16468 (NCI Thesaurus)
    C0009797 (UMLS 2011AA)
    CL Item
    Specific Protocol-related Issues (Specific protocol-related issues)
    CL Item
    Other Topics Discussed, Specify Below (Other Topics Discussed, specify below)
    Item
    Patient asked the following about this clinical trial (mark all that apply with an X)
    text
    Code List
    Patient asked the following about this clinical trial (mark all that apply with an X)
    CL Item
    Objectives; Significance Of Study (Objectives; Significance of study)
    CL Item
    Specific Treatment (Specific treatment)
    CL Item
    Medical Tests Required (Medical tests required)
    CL Item
    Side Effects (Side effects)
    CL Item
    What Patient Is Required To Do (What patient is required to do)
    CL Item
    Randomization Issues (Randomization issues)
    CL Item
    Other, Specify (Other, specify)
    Other,specify(patientaskedaboutthisclinicaltrial)
    Item
    Other, specify (patient asked about this clinical trial) (C.)
    text
    Item
    Consent Form (mark all that apply with an X)
    text
    Code List
    Consent Form (mark all that apply with an X)
    CL Item
    Interpreted/explained Language Used In Consent Form (Interpreted/explained language used in consent form)
    CL Item
    Patient Can Leave Study At Any Time Without Repercussions (Patient can leave study at any time without repercussions)
    CL Item
    The Right Of The Patient To Contact A Person In The Hospital If She Feels Her Rights Have Not Been Protected (The right of the patient to contact a person in the hospital if she feels her rights have not been protected)
    Item
    Specific protocol-related issues (mark all that apply with an X)
    text
    Code List
    Specific protocol-related issues (mark all that apply with an X)
    CL Item
    Transportation To/from Hospital (Transportation to/from hospital)
    CL Item
    Whether Costs Of Participation In Study Would Be Covered By Insurance (Whether costs of participation in study would be covered by insurance)
    CL Item
    Confidentiality Of Data (Confidentiality of data)
    CL Item
    Other, Specify (Other, specify)
    Other,specify(specificprotocol-relatedissues)
    Item
    Other, specify (specific protocol-related issues) (E.)
    text
    OtherTopicsDiscussed,specifybelow
    Item
    Other Topics Discussed, specify below
    text
    CALGBForm
    Item
    CALGB Form
    text
    CALGBForm
    Item
    CALGB Form
    text
    Y-MEPatientID
    Item
    Y-ME Patient ID (6.)
    text
    Y-MEPatientID
    Item
    Y-ME Patient ID (6.)
    text
    Item Group
    Telephone Interview
    C0021823 (UMLS CUI-1)
    (UMLS CUI-2)
    Item
    What were the patient's concerns about participating in this clinical trial? (mark all that apply)
    text
    C2699424 (UMLS CUI-1)
    C0681850 (UMLS CUI-2)
    Code List
    What were the patient's concerns about participating in this clinical trial? (mark all that apply)
    CL Item
    Didn't Understand The Study (a)
    CL Item
    Treatment Side Effects (b)
    CL Item
    Fear That Treatment Was Life-threatening (c)
    CL Item
    The Trial Was Not Asking An Important Question (d)
    CL Item
    Patient Felt That She Could Get Good Care Without Needing To Be On A Clinical Trial (e)
    CL Item
    Randomization; Wanted To Be On A Specific Arm Of The Trial (f)
    CL Item
    Didn't Understand The Consent Form (g)
    CL Item
    Was Frightened By The Consent Form (h)
    CL Item
    Transportation Not Available Or Too Expensive (i)
    CL Item
    Distance Need To Travel To Hospital Was Too Far (j)
    CL Item
    Costs Of Treatment That Would Not Be Covered By Insurance (k)
    CL Item
    Confidentiality Of Medical Records (l)
    CL Item
    Afraid Of Oncologist's Reaction If She Decided Not To Participate In Trial (m)
    CL Item
    Fears Of Family Members Or Friends Disapproving Of Her Decision About Participating In This Trial (n)
    CL Item
    Afraid Of Being A 'guinea Pig'; Treated By An Unproven Experimental Therapy (o)
    CL Item
    Insufficient Support At Home From Friends And Family To Help Patient While Being Treated (p)
    CL Item
    Other, Specify (q)
    CL Item
    Don't Know (r)
    Other concerns about trial participation
    Item
    Other, specify (patient's concerns about participating in this clinical trial)
    text
    Item
    Most Important (patient's concerns about participating in this trial)
    text
    Code List
    Most Important (patient's concerns about participating in this trial)
    CL Item
    Didn't Understand The Study (a)
    CL Item
    Treatment Side Effects (b)
    CL Item
    Fear That Treatment Was Life-threatening (c)
    CL Item
    The Trial Was Not Asking An Important Question (d)
    CL Item
    Patient Felt That She Could Get Good Care Without Needing To Be On A Clinical Trial (e)
    CL Item
    Randomization; Wanted To Be On A Specific Arm Of The Trial (f)
    CL Item
    Didn't Understand The Consent Form (g)
    CL Item
    Was Frightened By The Consent Form (h)
    CL Item
    Transportation Not Available Or Too Expensive (i)
    CL Item
    Distance Need To Travel To Hospital Was Too Far (j)
    CL Item
    Costs Of Treatment That Would Not Be Covered By Insurance (k)
    CL Item
    Confidentiality Of Medical Records (l)
    CL Item
    Afraid Of Oncologist's Reaction If She Decided Not To Participate In Trial (m)
    CL Item
    Fears Of Family Members Or Friends Disapproving Of Her Decision About Participating In This Trial (n)
    CL Item
    Afraid Of Being A 'guinea Pig'; Treated By An Unproven Experimental Therapy (o)
    CL Item
    Insufficient Support At Home From Friends And Family To Help Patient While Being Treated (p)
    CL Item
    Other, Specify (q)
    CL Item
    Don't Know (r)
    Item
    2nd Most Important (patient's concerns about participating in this trial)
    text
    Code List
    2nd Most Important (patient's concerns about participating in this trial)
    CL Item
    Didn't Understand The Study (a)
    CL Item
    Treatment Side Effects (b)
    CL Item
    Fear That Treatment Was Life-threatening (c)
    CL Item
    The Trial Was Not Asking An Important Question (d)
    CL Item
    Patient Felt That She Could Get Good Care Without Needing To Be On A Clinical Trial (e)
    CL Item
    Randomization; Wanted To Be On A Specific Arm Of The Trial (f)
    CL Item
    Didn't Understand The Consent Form (g)
    CL Item
    Was Frightened By The Consent Form (h)
    CL Item
    Transportation Not Available Or Too Expensive (i)
    CL Item
    Distance Need To Travel To Hospital Was Too Far (j)
    CL Item
    Costs Of Treatment That Would Not Be Covered By Insurance (k)
    CL Item
    Confidentiality Of Medical Records (l)
    CL Item
    Afraid Of Oncologist's Reaction If She Decided Not To Participate In Trial (m)
    CL Item
    Fears Of Family Members Or Friends Disapproving Of Her Decision About Participating In This Trial (n)
    CL Item
    Afraid Of Being A 'guinea Pig'; Treated By An Unproven Experimental Therapy (o)
    CL Item
    Insufficient Support At Home From Friends And Family To Help Patient While Being Treated (p)
    CL Item
    Other, Specify (q)
    CL Item
    Don't Know (r)
    Item
    3rd Most Important (patient's concerns about participating in this trial)
    text
    Code List
    3rd Most Important (patient's concerns about participating in this trial)
    CL Item
    Didn't Understand The Study (a)
    CL Item
    Treatment Side Effects (b)
    CL Item
    Fear That Treatment Was Life-threatening (c)
    CL Item
    The Trial Was Not Asking An Important Question (d)
    CL Item
    Patient Felt That She Could Get Good Care Without Needing To Be On A Clinical Trial (e)
    CL Item
    Randomization; Wanted To Be On A Specific Arm Of The Trial (f)
    CL Item
    Didn't Understand The Consent Form (g)
    CL Item
    Was Frightened By The Consent Form (h)
    CL Item
    Transportation Not Available Or Too Expensive (i)
    CL Item
    Distance Need To Travel To Hospital Was Too Far (j)
    CL Item
    Costs Of Treatment That Would Not Be Covered By Insurance (k)
    CL Item
    Confidentiality Of Medical Records (l)
    CL Item
    Afraid Of Oncologist's Reaction If She Decided Not To Participate In Trial (m)
    CL Item
    Fears Of Family Members Or Friends Disapproving Of Her Decision About Participating In This Trial (n)
    CL Item
    Afraid Of Being A 'guinea Pig'; Treated By An Unproven Experimental Therapy (o)
    CL Item
    Insufficient Support At Home From Friends And Family To Help Patient While Being Treated (p)
    CL Item
    Other, Specify (q)
    CL Item
    Don't Know (r)
    Item
    What was the outcome at the end of the call? (mark all that apply with an X)
    text
    Code List
    What was the outcome at the end of the call? (mark all that apply with an X)
    CL Item
    Patient Decided To Participate In Trial (Patient decided to participate in trial)
    CL Item
    Patient Decided Not To Participate (Patient decided not to participate)
    CL Item
    Patient Would Continue To Think About Whether To Participate (Patient would continue to think about whether to participate)
    CL Item
    Arranged To Speak Again To The Patient (Arranged to speak again to the patient)
    CL Item
    Sent Some Information Brochures To The Patient [specify Which:] (Sent some information brochures to the patient [specify which:])
    CL Item
    Referred Patient To Another Agency/professional Concerning Matters Other Than Their Participation In This Clinical Trial (Referred patient to another agency/professional concerning matters other than their participation in this clinical trial)
    CL Item
    Suggested Patient Speak With A Member Of Their Medical Team Where She Is Being Treated (Suggested patient speak with a member of their medical team where she is being treated)
    CL Item
    Other, Specify (Other, specify)
    Information brochure
    Item
    Sent some information brochures to the patient [specify which:]
    text
    C0030258 (UMLS CUI-1)
    Other,specify(outcomeattheendofthecall)
    Item
    Other, specify (outcome at the end of the call)
    text
    CompletedBy
    Item
    Completed By (Print or Type Name)
    text
    Date completed
    Item
    Date Completed
    date
    C0011008 (UMLS CUI-1)

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