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Active, not recruitingNCT06184919Updated Feb 12, 2026

Preparing Older Adults for Major Surgery With Preoperative Comprehensive Geriatric Assessments

An observational study in Surgery, Aging and Health Care Utilization, sponsored by University of Wisconsin, Madison. Active, not recruiting at 1 site in United States. Per ClinicalTrials.gov, last updated 2026-02-12.

Sponsored by University of Wisconsin, Madison · Observational

Study type
Observational
Model
Other
Time perspective
Prospective
Enrollment
50
Sex
All
01

Study summary

The researchers will conduct observations, interviews, and focus groups with clinicians, staff and patients of the Perioperative Optimization of Senior Health (POSH) clinic, which conducts preoperative comprehensive geriatric assessments (pCGA) at UW Health to understand clinic processes and potential areas for improvement. The goal is to (1) create a process map describing clinic workflow and (2) redesign the process with healthcare providers and patients/families.

Read the detailed description

Aim 1: Process mapping using direct observation, interviews and focus groups to identify opportunities for system redesign

The research team will directly observe n=30 patients in POSH clinic visits, taking notes and documenting the persons, tasks, tools/technologies, environment and organizational factors affecting healthcare delivery. Observer notes will be supplemented with audio recording of the clinic visit. Observations will also include assessments performed by social workers, pharmacist, medical assistants.

Semi-structured qualitative interviews with patients who participated in the observations and their caregivers, if any, will be conducted 2 weeks after the pCGA visit. Interviewers will assess barriers, facilitators, motivation, and adherence to tasks, and reflections on the process of scheduling, attending and participating in the clinic. Surgeons who refer patients (n=20) will be interviewed using semi-structured guides to elicit feedback on the process map and explore perceived barriers and facilitators to adoption of the pCGA.

Focus Groups: Healthcare professionals and staff (n=20) who conduct the pcga will participate in a focus group to provide feedback on the process map. The researchers will elicit feedback on the process map, clarifying its accuracy as a representation of the tasks and procedures performed, and identifying system-level barriers and facilitators at each step.

Aim 2: Co-design an implementation package for the pCGA at (2a) a large academic hospital and (2b) an affiliate community site.

The research team will apply user-centered participatory design methods to adapt the process map (aim 1) into an implementation package, which consists of a set of implementation strategies, to address barriers and enhance facilitators at each step. Participatory design (also called "co-design") is a systems engineering approach where the researchers and participants work together in designing the workflow of an intervention. Co-design sessions will be conducted in parallel at our University Hospital (2a) and a local affiliated community hospital (2b). There will be two groups (design teams) of patients/caregivers and healthcare professionals per location, for a total of four groups.

This study will include five co-design videoconference sessions with up to n=10 members in each group (total n=40) over approximately 6 months, with 2-3 weeks between each session. Each session will last 90 minutes. The sessions will identify process changes that can address barriers and facilitators to promote implementation of the pCGA. The research team will analyze audio recordings and notes from each session. These findings will be synthesized and presented at the next design session. Each design team will participate in sessions independently, however, the research team will summarize output from each session and provide this content to the alternate design team for comment.

Design sessions are expected to generate an implementation package that is ready for feasibility and pilot testing at the University hospital. Design sessions at the community site will serve as a template for implementation at a future date.

02

Conditions studied

  • Surgery
  • Aging
  • Health Care Utilization
  • Frailty

Keywords

  • Human Factors Engineering
  • Perioperative Optimization
03

In context

Patient Acceptance of Health Care

93 studies on the registry are indexed under Patient Acceptance of Health Care; 30 are open to participants now.

This study's enrollment of 50 is below the median of 236 across 18 observational studies indexed under Patient Acceptance of Health Care.

Browse Patient Acceptance of Health Care studies →

Lead sponsor

University of Wisconsin, Madison is the lead sponsor of 1,161 studies on the registry; 182 are open to participants now.

Of its 151 completed or terminated interventional studies of FDA-regulated products, 114 (75%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Observations and Interviews in the Perioperative Optimization of Senior Health (POSH) clinic.

Inclusion criteria

  • Being a patient seen for a pCGA clinic at the time of observations, or being the caregiver of such a patient.
  • Being a clinician or staff member working at the pCGA clinic
  • Being a surgeon who frequently refers patients to the pCGA clinic

Exclusion criteria

Exclusion Criteria:

  • For patients:

    • not being fluent in English
    • having an enacted power of attorney indicating that the patient is unable to make medical decisions for themselves and a legally authorized representative (LAR) does not attend the pCGA visit with the patient
  • For pCGA clinicians and staff: none
  • For surgeons: none
05

Study design

Observational model
Other
Time perspective
Prospective
Enrollment
50 participants (actual)
Patient registry
No

Groups and cohorts

  • Patients and caregivers

    Patients attending the Perioperative Optimization of Senior Health (POSH) clinic

    Other: Process Mapping: Observations · Other: Process Mapping: Interviews · Other: Participatory Design

  • Healthcare providers

    Healthcare providers referring to or working in the Perioperative Optimization of Senior Health (POSH) clinic

    Other: Process Mapping: Observations · Other: Process Mapping: Interviews · Other: Process Mapping: Focus Group · Other: Participatory Design

Interventions

  • OtherProcess Mapping: Observations

    Direct observations of the POSH clinic visit.

  • OtherProcess Mapping: Interviews

    Semi-structured interviews of patients and providers involved in the POSH clinic.

  • OtherProcess Mapping: Focus Group

    Focus group of providers and staff who conduct the POSH clinic.

  • OtherParticipatory Design

    Participatory design, also called "co-design" is a systems engineering approach where the researchers and participants work together in designing the workflow of an intervention. There will be two groups (design teams) of patients/caregivers and healthcare professionals per location, for a total of four groups.

06

What researchers measure

Primary outcomes

  1. Process map

    The direct observations, interviews and focus groups conducted with patients and caregivers will help create a detailed process map of preoperative geriatric assessments. Specifically this map will detail the persons, tasks, tools/technologies, environment and organizational factors involved in the process according to the System Engineering Initiative for Patient Safety model.

    Time frame: 12 months

  2. Implementation Package

    Co-design sessions will generate an implementation package, consisting of a set of implementation strategies, that can be piloted for its feasibility and adapted to facilitate preoperative comprehensive geriatric assessment in other settings.

    Time frame: 24 months

Secondary outcomes

  1. Qualitative data: Barriers and Facilitators to preoperative comprehensive geriatric assessments

    The qualitative analysis performed of interviews and focus groups during process mapping will identify barriers and facilitators to the use of preoperative comprehensive geriatric assessments.

    Time frame: 5 years

07

Study locations

1 site
  • UW Hospital and Clinics
    Madison, Wisconsin 53792, United States
08

References and documents

Individual participant data

Plan to share: No

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 12, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06184919
Lead sponsor
University of Wisconsin, Madison
Collaborators
National Institute on Aging (NIA)
Responsible party
Sponsor
First posted
Dec 29, 2023
Start date
Jun 14, 2023
Primary completion
Sep 30, 2026 (estimated)
Completion
Apr 30, 2028 (estimated)
Last update
Feb 12, 2026

Study contacts

Julia R Berian, MD
principal investigator · University of Wisconsin, Madison

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is active, not recruiting, as verified in Feb 2026. You cannot join it, but the record below documents what was studied.

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