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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04514523
Other study ID # 2000026483
Secondary ID 1R21AG061427-011
Status Completed
Phase N/A
First received
Last updated
Start date April 28, 2020
Est. completion date September 22, 2020

Study information

Verified date December 2022
Source Yale University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to co-develop a toolkit (known as the QBSAfe toolkit) with patients, family caregivers, and clinicians that focuses on palliating symptoms, alleviating burden of treatment, facilitating social connections, and optimizing treatment safety for patients with diabetes mellitus.


Recruitment information / eligibility

Status Completed
Enrollment 91
Est. completion date September 22, 2020
Est. primary completion date September 22, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: -Existing diagnosis of diabetes mellitus; have an existing appointment with a participating clinician Exclusion Criteria: - Do not speak English - Severe vision/hearing impairment - Unable to give informed consent for any reason

Study Design


Related Conditions & MeSH terms


Intervention

Other:
QBSAfe Toolkit
The QBSAfe toolkit focuses on palliating symptoms, alleviating burden of treatment, facilitating social connections, and optimizing treatment safety.

Locations

Country Name City State
United States Yale University New Haven Connecticut
United States Mayo Clinic Rochester Minnesota
United States Trinity Health of New England Waterbury Connecticut

Sponsors (4)

Lead Sponsor Collaborator
Yale University National Institute on Aging (NIA), National Institutes of Health (NIH), Trinity Health of New England

Country where clinical trial is conducted

United States, 

References & Publications (1)

Clark JE, Boehmer KR, Breslin M, Haider S, Pasciak W, Gravholt D, Sanchez BB, Hartasanchez SA, El Kawkgi OM, Montori V, Lipska KJ. Quality of life, burden of treatment, safety, and avoidance of future events (QBSAfe) protocol: a pilot study testing an intervention to shift the paradigm of diabetes care. Pilot Feasibility Stud. 2021 Nov 8;7(1):196. doi: 10.1186/s40814-021-00935-8. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Acceptability - Patients Patient responses to post-visit questionnaires. Baseline [Post Clinical Encounter]
Primary Acceptability - Clinicians Clinician responses to post-visit questionnaires. Baseline [Post Clinical Encounter]
Secondary Feasibility 1 Percentage of participants who completed the study procedures. Baseline [Post Clinical Encounter]
Secondary Feasibility 2 Percentage of recorded visits in which the QBSAFE toolkit was used assessed by Number of visits QBSAFE was used/Number of recorded visits. Baseline [Post Clinical Encounter]
Secondary Feasibility 3 Time to recruit 84 subjects across 3 sites. Baseline [Post Clinical Encounter]
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