- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07793708
Older Adults' Recovery Dynamics After Cardiac Surgery (ODYSSEY)
Clinical, Functional, and Biological Characterization of Resilience in Older Adults Undergoing Cardiac Surgery: ODYSSEY Study - Pilot Phase
Population aging has increased the number of older adults exposed to interventions with high physiological demand, which are associated with frequent adverse outcomes such as delirium, organ dysfunction, and delayed functional recovery. Current clinical tools, such as frailty assessments, help identify higher-risk populations but do not adequately explain the marked individual variability in recovery or accurately predict who will develop complications. This variability may be partly explained by individual resilience, defined as the ability to recover toward, return to, or even surpass a prior functional state after an acute stressor. Evidence suggests that biological mechanisms related to aging influence resilience; however, biomarkers and integrated clinical models capable of characterizing and potentially modulating resilience in humans remain limited. Therefore, a standardized clinical platform is needed to characterize physiological resilience and its determinants, generating actionable knowledge to improve risk stratification, guide interventions, and optimize recovery in older adults.
To this end, a single-center prospective cohort study will be conducted at Clinica Bicentenario Santiago, including individuals aged ≥65 years who are independent or have mild dependency and are undergoing elective cardiac surgery requiring sternotomy for valvular and/or coronary artery disease, recruited between 2026 and 2027. Participants will undergo a baseline assessment 2-3 weeks before surgery; an early postoperative assessment focused on the systematic recording of clinical outcomes, including delirium and organ dysfunction; and longitudinal follow-up to characterize recovery after discharge. Follow-up assessments will include frailty, intrinsic capacity (the composite of an individual's physical and mental capacities across the cognitive, locomotor, psychological, vitality, and sensory domains), functional status, health-related quality of life, and perceived fatigability, according to the prespecified assessment schedule.
In addition, blood samples will be collected at three time points (baseline, 24 hours postoperatively, and one month after surgery) to measure plasma levels of growth differentiation factor 15 (GDF-15), a biomarker associated with aging-related biological stress and systemic responses to tissue injury. It is projected that at least 75 participants will be recruited over a 12-month period, allowing characterization of baseline clinical and functional profiles, the frequency of postoperative complications and organ dysfunction, trajectories of recovery, and associations between baseline characteristics, biological markers, and subsequent recovery outcomes.
Study Overview
Status
Conditions
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Felipe H Salech, MD PhD
- Phone Number: +56998739448
- Email: fhsalech@gmail.com
Study Locations
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Santiago, Chile
- Clinica Bicentenario Red Salud
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Contact:
- Felipe Salech, MD PhD
- Phone Number: +56998739448
- Email: fhsalech@gmail.com
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Older adults (≥ 65 años) undergoing elective cardiac surgery via median sternotomy, including coronary artery bypass grafting (CABG) and/or valvular surgery.
- Independence in basic daily activities, defined as a Barthel Index score ≥80.
Exclusion Criteria:
- Emergency surgery for any indication
- Terminal illness, defined as a life expectancy of less than 12 months
- History of cognitive impairment, defined as a documented diagnosis of dementia and/or current treatment with memantine or donepezil
- Advanced hepatic or renal failure, defined as Child-Pugh class C liver disease or chronic dialysis
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Frailty
Time Frame: 1 month after discharge
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Frailty measured by the Physical Frailty Phenotype (Fried Frailty Phenotype).
The total score ranges from 0 to 5, with higher scores indicating greater frailty.
Participants are classified as robust (score 0), prefrail (score 1-2), or frail (score 3-5).
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1 month after discharge
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Functional status assessed by the Barthel Index
Time Frame: 1, 6, and 12 months after discharge
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Functional status in basic activities of daily living will be assessed using the Barthel Index.
The total score ranges from 0 to 100 points, with higher scores indicating greater independence in basic activities of daily living and therefore better functional status.
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1, 6, and 12 months after discharge
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Functional status assessed by the Lawton-Brody Instrumental Activities of Daily Living Index
Time Frame: 1, 6, and 12 months after hospital discharge
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Functional status in instrumental activities of daily living will be assessed using the Lawton-Brody Instrumental Activities of Daily Living Index.
The scale evaluates independence in instrumental activities of daily living, with higher scores indicating greater independence and therefore better functional status.
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1, 6, and 12 months after hospital discharge
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Cognitive capacity assessed by the Montreal Cognitive Assessment
Time Frame: 1 month after hospital discharge
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Cognitive capacity will be assessed using the Montreal Cognitive Assessment (MoCA), a cognitive screening instrument evaluating multiple cognitive domains.
The total score ranges from 0 to 30 points, with higher scores indicating better cognitive performance.
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1 month after hospital discharge
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Cognitive capacity assessed by the AD8 Dementia Screening Interview
Time Frame: 1 month after hospital discharge
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Cognitive capacity will also be assessed using the AD8 Dementia Screening Interview (AD8), an 8-item screening instrument for cognitive change.
The total score ranges from 0 to 8 points, with higher scores indicating greater cognitive impairment and therefore a worse outcome.
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1 month after hospital discharge
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Locomotor capacity assessed by the Short Physical Performance Battery
Time Frame: 1 month after hospital discharge
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Locomotor capacity will be assessed using the Short Physical Performance Battery (SPPB), which evaluates standing balance, gait speed, and repeated chair stands.
The total score ranges from 0 to 12 points, with higher scores indicating better physical performance.
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1 month after hospital discharge
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Psychological capacity assessed by the Patient Health Questionnaire-9
Time Frame: 1 month after hospital discharge
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Psychological capacity will be assessed using the Patient Health Questionnaire-9 (PHQ-9), a 9-item instrument assessing depressive symptoms.
The total score ranges from 0 to 27 points, with higher scores indicating greater severity of depressive symptoms and therefore a worse outcome.
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1 month after hospital discharge
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Vitality assessed by the Mini Nutritional Assessment-Short Form
Time Frame: 1 month after hospital discharge
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Vitality will be assessed using the Mini Nutritional Assessment-Short Form (MNA-SF), a nutritional screening instrument for older adults.
The total score ranges from 0 to 14 points, with higher scores indicating better nutritional status.
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1 month after hospital discharge
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Visual capacity assessed by the Integrated Care for Older People vision screening tool
Time Frame: 1 month after hospital discharge
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Visual capacity will be assessed using the World Health Organization Integrated Care for Older People (ICOPE) vision screening tool.
Participants will be classified according to the ICOPE screening assessment as having no evidence of visual impairment or evidence of visual impairment.
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1 month after hospital discharge
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Hearing capacity assessed by the Integrated Care for Older People hearing screening tool
Time Frame: 1 month after hospital discharge
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Hearing capacity will be assessed using the World Health Organization Integrated Care for Older People (ICOPE) hearing screening tool.
Participants will be classified according to the ICOPE screening assessment as having no evidence of hearing impairment or evidence of hearing impairment.
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1 month after hospital discharge
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Perceived fatigability assessed by the Pittsburgh Fatigability Scale
Time Frame: 1 month after hospital discharge
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Perceived fatigability will be assessed using the Pittsburgh Fatigability Scale (PFS), which evaluates anticipated physical and mental fatigue associated with 10 standardized activities.
Each activity is rated from 0 to 5 points, with 0 indicating no fatigue and 5 indicating extreme fatigue.
Physical fatigability and mental fatigability are scored separately, each ranging from 0 to 50 points.
Higher scores indicate greater perceived fatigability and therefore a worse outcome.
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1 month after hospital discharge
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Health-related quality of life assessed by the EuroQol 5-Dimension 3-Level questionnaire
Time Frame: 1 month after hospital discharge
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Health-related quality of life will be assessed using the EuroQol 5-Dimension 3-Level (EQ-5D-3L) questionnaire.
The descriptive system evaluates five dimensions: mobility, self-care, usual activities, pain/discomfort, and anxiety/depression.
Each dimension has three response levels: no problems, some or moderate problems, and extreme problems.
In addition, participants will rate their overall health using the EuroQol Visual Analogue Scale (EQ VAS), which ranges from 0 to 100, with higher scores indicating better perceived health status.
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1 month after hospital discharge
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Organ dysfunction severity assessed by the Sequential Organ Failure Assessment score
Time Frame: During the first 4 postoperative days
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Organ dysfunction severity will be assessed using the Sequential Organ Failure Assessment (SOFA) score, which evaluates respiratory, coagulation, hepatic, cardiovascular, central nervous system, and renal function.
The total score ranges from 0 to 24 points, with higher scores indicating greater organ dysfunction and therefore a worse outcome.
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During the first 4 postoperative days
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Postoperative Delirium
Time Frame: During the first 4 postoperative days
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Presence of postoperative delirium assessed during the immediate postoperative period using standardized clinical criteria.
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During the first 4 postoperative days
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Survival
Time Frame: Up to 12 months after hospital discharge.
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All-cause mortality.
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Up to 12 months after hospital discharge.
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Growth Differentiation Factor 15 (GDF-15)
Time Frame: 24 hours after cardiac surgery and 1 month after hospital discharge
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Plasma levels of Growth Differentiation Factor 15 (GDF-15) measured as a biomarker of biological stress and resilience.
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24 hours after cardiac surgery and 1 month after hospital discharge
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- P-42.2025
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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