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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02986958
Other study ID # R21AG049967
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date August 2016
Est. completion date August 2017

Study information

Verified date December 2018
Source Johns Hopkins Bloomberg School of Public Health
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study evaluates an agenda-setting checklist for patients with cognitive impairment and their family companions that is completed in the waiting room in advance of a primary care visit. The study team will conduct a two-group randomized trial to examine feasibility of the protocol and to compare medical communication (from visit audiotapes) during visits of patient-companion dyads who complete the checklist (n=50) with patient-companion dyads who receive usual care (n=50)


Description:

The study team has established proof of concept for a paper-pencil checklist to be used by older patients and their companions in the waiting room prior to medical visits. The checklist is designed to elicit and align patient and companion perspectives regarding patient health issues to discuss with the doctor, and to stimulate discussion about the companion's role in the visit. The premise for the checklist is that companions are typically motivated to support patients during medical visits, but that they often lack knowledge of the patient's health concerns and preferences for communication assistance.

The study team will conduct a two group pilot randomized trial of up to 100 (50 per group) patients ages 65+ with cognitive impairment and their unpaid companion to test the effects of the refined checklist for medical communication. Each patient-companion dyad will be randomized to the intervention (to receive the checklist) or to a control protocol. The study will evaluate the feasibility of delivering the study protocol to patients with cognitive impairment and their companions in primary care, and to generate preliminary evidence regarding the effect of the checklist on medical communication. For these reasons, the control group protocol will comprise usual care which is in this case existing clinical practice. Patients (when feasible), companions, and doctors in both intervention and control groups will complete in-person post-visit surveys immediately after the visit. Patients (when feasible) and companions will separately complete follow-up surveys by telephone two weeks after the doctor visit conducted by a research staff member.


Recruitment information / eligibility

Status Completed
Enrollment 93
Est. completion date August 2017
Est. primary completion date August 2017
Accepts healthy volunteers No
Gender All
Age group 65 Years and older
Eligibility Inclusion Criteria:

- Older adults: 65 years or older, established patient of participating primary care provider, regularly attend medical visits with one or more family member or unpaid friend "companion(s)", agree to allow companion to be contacted and participate in the study, authorize disclosure of Protected Health Information (PHI) in their electronic health record, able to provide informed consent or have a legally authorized representative

- Companion: family member (spouse, adult child, parent, adult sibling) or unpaid friend who accompanies older adult participant to medical visits.

- Primary care provider: practicing physician, nurse practitioner or physician assistant at a participating primary care practice.

Exclusion Criteria:

- Older adults: younger than 65 years, no evidence of cognitive impairment, do not attend medical visits with family member or unpaid friend.

- Companion: paid non-family member who accompanies patient to visits

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Pre-visit patient-family agenda-setting checklist
Pre-visit patient-family agenda-setting checklist
Usual care
routine primary care

Locations

Country Name City State
United States Johns Hopkins Community Physicians Aberdeen Maryland
United States Medstar Center for Successful Aging Baltimore Maryland
United States Johns Hopkins Community Physicians Westminster Maryland

Sponsors (3)

Lead Sponsor Collaborator
Johns Hopkins Bloomberg School of Public Health Johns Hopkins Community Physicians, Medstar Health Research Institute

Country where clinical trial is conducted

United States, 

References & Publications (2)

Wolff JL, Guan Y, Boyd CM, Vick J, Amjad H, Roth DL, Gitlin LN, Roter DL. Examining the context and helpfulness of family companion contributions to older adults' primary care visits. Patient Educ Couns. 2017 Mar;100(3):487-494. doi: 10.1016/j.pec.2016.10.022. Epub 2016 Oct 25. — View Citation

Wolff JL, Roter DL, Barron J, Boyd CM, Leff B, Finucane TE, Gallo JJ, Rabins PV, Roth DL, Gitlin LN. A tool to strengthen the older patient-companion partnership in primary care: results from a pilot study. J Am Geriatr Soc. 2014 Feb;62(2):312-9. doi: 10.1111/jgs.12639. Epub 2014 Jan 13. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Ratio of Psychosocial and Socio-emotional Statements Relative to Biomedical Talk and Orientation Statements (Patient-Centered Communication) Patient-centered communication is reflected as a ratio of psychosocial and socio-emotional statements relative to biomedical talk and orientation statements from coded audio-taped communication during primary care visits. Higher values indicate more patient-centered communication. During enrollment visit, up to 77 minutes
Secondary Visit Duration Duration of primary care visit in minutes During enrollment visit, up to 77 minutes
Secondary Patient Verbal Activity Patient verbal activity is the proportion of visit statements contributed by the patient in relation to overall visit statements, including statements by the companion and primary care provider. During enrollment visit, up to 77 minutes
Secondary Companion Verbal Activity Companion verbal activity is the proportion of visit statements contributed by the companion in relation to overall visit statements, including statements by the patient and primary care provider. During enrollment visit, up to 77 minutes
Secondary Number of Participants for Whom There Was Any Discussion of the Patient's Memory and/or Cognition During the Primary Care Visit The number of participants for whom there was any discussion of the patient's memory and/or cognition during the audio-recorded primary care visit. During enrollment visit, up to 77 minutes
Secondary Number of Patients Who Agree or Strongly Agree With Being Satisfied With the Primary Care Visit The number of patients who endorsed "Agree" or "Strongly Agree" to the statement: "Overall, I was satisfied with today's visit." During Enrollment visit, up to 77 minutes
Secondary Number of Companions Who Agree or Strongly Agree With Being Satisfied With the Primary Care Visit The number of companions who endorsed "Agree" or "Strongly Agree" to the statement: "Overall, I was satisfied with today's visit." During Enrollment visit, up to 77 minutes
Secondary Number of Primary Care Providers Who Agree or Strongly Agree With Being Satisfied With the Primary Care Visit The number of primary care providers who endorsed "Agree" or "Strongly Agree" to the statement: "Overall, I was satisfied with today's visit." During Enrollment visit, up to 77 minutes
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