ClinicalTrials.gg
Not yet recruitingNCT07764289POPUpdated Aug 13, 2026

The Perioperative Pathway for Older Adults

An observational study in Older Adults (65 Years and Older), Postoperative Care and Preoperative Care, sponsored by Örebro University, Sweden. Not yet recruiting. Open to participants aged 65 Years and older. Per ClinicalTrials.gov, last updated 2026-08-13.

Sponsored by Örebro University, Sweden · Observational

Study type
Observational
Model
Other
Time perspective
Prospective
Enrollment
1,000,000
Ages
65 Years and older
Sex
All
01

Study summary

More than 1.5 million people undergo surgery in Sweden each year, and over 770,000 of them are aged 65 years or older. Older adults often have more complex health needs and may require additional support throughout the surgical care process.

Surgical care can be divided into three phases: before, during, and after surgery. Before surgery, older adults may need to improve their health status and prepare for the procedure. Many also feel worried about the surgery and recovery. It is important that patients understand the information they receive and are involved in decisions about their care. However, some older adults find it difficult to understand health information or to ask questions, which can make participation in care more challenging.

Recovery after surgery means returning to the same level of function as before surgery, or adjusting to a new level if needed. For older adults, recovery can take longer and often continues after leaving the hospital. Support during this period is important for a safe and successful recovery.

The POP project aims to improve the care and support provided to older adults undergoing surgery. The project focuses on identifying gaps and differences in current care and improving support throughout the entire surgical pathway, regardless of the type of surgery.

There is currently limited knowledge about how older adults in Sweden experience the surgical care process. By increasing this understanding, the project aims to support improvements in care and outcomes for older adults.

02

Conditions studied

  • Older Adults (65 Years and Older)
  • Postoperative Care
  • Preoperative Care
  • Intraoperative Care

Keywords

  • older adults
  • frail
  • mixed-method
  • perioperative period
03

In context

Lead sponsor

Örebro University, Sweden is the lead sponsor of 86 studies on the registry; 14 are open to participants now.

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

04

Who can participate

Ages eligible
65 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Older persons aged 65 or older. Next of kin and staff working at a nursing home.

Eligibility criteria

Preoperative concerns and health literacy

Inclusion Criteria:

  • 65 years and older
  • Being able to read and understand Swedish

Exclusion Criteria:

-Cognitive decline

Perioperative outcomes

Inclusion Criteria:

-65 years and older

Interviews with staff

Inclusion Critera:

-Working in a nursing home as a nurse assistant or a nurse with experience of pre- and postoperative care

Interviews with older persons and next-of-kin

Inclusion Criteria:

  • Living at a nursing home with an experience of undergoing surgery or being a next-of-kin to someone living at a nursing home
  • Being able to understand Swedish

Exclusion Criteria:

-Cognitive decline

05

Study design

Observational model
Other
Time perspective
Prospective
Enrollment
1,000,000 participants (estimated)
Target follow-up
12 Months
Patient registry
Yes

Groups and cohorts

  • Registry-based cohort

    Other: No intervention

  • Preoperative concerns and health literacy
  • Nurses and nurse assistants working in nursing homes

    Other: No intervention

  • Older adults and next of kin

    Other: No intervention

Interventions

  • OtherNo intervention

    No intervention

06

What researchers measure

Primary outcomes

  1. Preoperative concerns

    Preoperative concerns in older adults (PCOA) is a questionnaire developed by Li et al. PCOAS will be translated to Swedish and psychometrically evaluated. Minimum value 1, maximum value 5 per item and a higher score means higher concerns.

    Time frame: Before surgery.

  2. Interviews with older persons and next-of-kin

    The interviews will investigate how an older person living in a nursing home can be involved in their care before and after an operation.

    Time frame: The interview will be conducted at one time point approximately 60 minutes.

  3. Interviews with staff

    The interviews will investigate how is the perioperative care process for older people living in nursing homes perceived and organized from the perspective of the staff?

    Time frame: The interview will be conducted at one time point approximately 60 minutes.

  4. Health literacy

    The HLS19-Q12 ( (Health Literacy Population Survey 2019-2021) instrument will be used to measure general health literacy. HLS19-Q12 is scaled from 0 to 100. A higher score value signifies a higher level of general HL.

    Time frame: Before surgery.

Other outcomes

  1. Perioperative outcomes

    Surgical time in minutes

    Time frame: 12 months

  2. Perioperative outcomes

    The Swedish PeriOperative Registry (SPOR) includes perioperative data. Clinical Frailty Scale (CFS), minimum 1 and maximum 9, with a cutoff of 4 will be used to classify high vs. low frailty .

    Time frame: 12 month

  3. Perioperative outcomes.

    The Swedish PeriOperative Registry (SPOR) includes perioperative data. Quality of recovery-15 (QoR-15) minimum 0 and maximum 10 with a lower score indicating worse recovery, and mortality within 6 months ).

    Time frame: 12 month

  4. Perioperative outcomes

    Postoperative complications at the PACU: PONV yes/no, n(%), pain in numeric rating scale, POUR in milliliter, hypothermia in Celcius

    Time frame: Before discharge from the PACU

  5. Perioperative outcomes

    Lenght of stay in hours

    Time frame: At discharge from the PACU

  6. Perioperative outcomes

    Baseline data : age in yrs, height in meters, BMI kg/m\^2 , biological sex in n(%), ASA-classification in n(%), elective/acute surgery in n(%), intraoperative positioning in n(%)

    Time frame: Baseline

07

Study locations

No study locations are listed for this record.

08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 13, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07764289
Lead sponsor
Örebro University, Sweden
Responsible party
Maria Jaensson (Senior lecturer, Associate professor, Örebro University, Sweden) — Principal investigator
First posted
Aug 13, 2026
Start date
Oct 2026 (estimated)
Primary completion
Jan 2030 (estimated)
Completion
Jan 2030 (estimated)
Last update
Aug 13, 2026

Study contacts

Maria Jaensson
Contact
maria.jaensson@oru.se
+4619303405

Oversight

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

Not currently enrolling

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

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion