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PROMs-guided Perioperative Care in Patients With Complex Care Needs: An Open-label Randomized Controlled Trial

Optimization of the Perioperative Pathway Coordinated Through the Collection of Patient-reported Outcome Measures in Patients With Complex Care Needs: An Open-label Randomized Controlled Trial

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07338188
Acronym
OPTICAIRE
Enrollment
276
Registered
2026-01-13
Start date
2025-12-31
Completion date
2028-04-03
Last updated
2026-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Postoperative Follow-up

Keywords

perioperative, surgery, Patient Reported Outcomes Mesuares (PROMs), Complex clinical situation

Brief summary

This research aims to identify, as early as the preoperative phase, groups of patients likely to experience maximum clinical improvement through structured paramedical follow-up based on PROMs. However, the high heterogeneity of the included patients could have masked more pronounced effects in certain subgroups, particularly those at higher risk. Relying on a multicenter approach and a subgroup analysis, our study hypothesizes that certain patient profiles are more likely to significantly benefit from personalized follow-up based on PROMs. The objective is to validate the hypothesis that support through PROMs for patients in complex situations could allow for a more pronounced clinical effect. This follow-up will enable better targeting of interventions from the preoperative phase, optimize the use of healthcare resources, and improve quality, safety, and efficiency of perioperative pathways.

Detailed description

The study is an open-label, multicenter, randomized controlled trial comparing two groups: * A control group receiving the usual conventional follow-up, notably by the surgeon and the attending physician. * An experimental group receiving, in addition to the usual conventional follow-up, follow-up by dedicated nurses focusing on the patient's perspective regarding their health status (OPTIMISTE follow-up).

Interventions

Description - Patient-Reported Outcomes-based perioperative follow-up (QoR-15 focus) The Patient-Reported Outcomes-based perioperative follow-up is a patient-centered approach that evaluates postoperative recovery using standardized questionnaires completed directly by the patient. This method highlights the patient's own perception of recovery-covering physical comfort, emotional state, independence, and pain control-rather than relying solely on clinical or physiological parameters. The Quality of Recovery-15 (QoR-15) questionnaire is a validated, short-form tool designed to measure the quality of postoperative recovery from the patient's perspective. It consists of 15 items covering five key dimensions: Physical comfort (pain, nausea, general well-being), Emotional state (anxiety, depression, feeling of support), Psychological support, Physical independence (ability to move or perform daily activities), Pain and symptom management.

Sponsors

University Hospital, Strasbourg, France
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Male or female * Adult patient, with no upper age limit * Undergoing scheduled or unscheduled surgery in a center participating in the research * Presenting a care situation identified as complex, defined by a COMID score \> 9 * Subject affiliated to a social health insurance scheme * Subject able to understand the objectives and risks related to the research and to give informed consent, dated and signed

Exclusion criteria

* Inability to administer the mQoR-15f questionnaire (cognitive disorders, language barrier) * Inability to provide the subject with informed information (subject in an emergency situation, difficulties in understanding, etc.) * Patient who has already received previous follow-up by the OPTIMISTE team * Patient enrolled in a therapeutic trial that may affect post-operative recovery quality * Subject under legal protection, guardianship or curatorship * Pregnant or breastfeeding woman

Design outcomes

Primary

MeasureTime frameDescription
The main objective is to evaluate the effectiveness of a perioperative follow-up integrating the patient's perspective based on their perceived health status.Between the baseline consultation and day 35Evolution of a modified version of the French Quality-Of-Recovery 15 score (QoR-15f) between the baseline consultation and postoperative day 35 (depending on the groups: with or without the OPTISMISTE program). The evoluation is scored from 0 to 150 (A higher score indicates better quality of recovery.)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026