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Active, not recruitingNCT07471945Updated Apr 22, 2026

Individualized Nursing Care and Frailty Outcomes in Cardiac Surgery

An interventional study of Experimental in Frail Patient, Cardiac Surgical Procedures (Postoperative Population) and Patient-centered Care, sponsored by SELDA MERT. Active, not recruiting at 1 site in Turkey (Türkiye). Open to participants aged 65 Years and older. Per ClinicalTrials.gov, last updated 2026-04-22.

Sponsored by SELDA MERT · Not applicable, Interventional, and Supportive care

From the registry’s dates

  • Primary completion was expected by Apr 2026, 5 months ago, but the record still lists the study as active, not recruiting.
Phase
Not applicable
Study type
Interventional
Enrollment
75
Allocation
Randomized
Ages
65 Years and older
Sex
All
01

Study summary

This study is a randomized controlled trial aiming to compare targeted individualized nursing care with standard care in frail elderly patients undergoing cardiac surgery.

The hypotheses of the study are:

H1: Targeted individualized nursing care has an effect on the frailty level of frail elderly patients undergoing cardiac surgery.

H2: Targeted individualized nursing care affects the factors influencing frailty in frail elderly patients undergoing cardiac surgery.

02

Conditions studied

  • Frail Patient
  • Cardiac Surgical Procedures (Postoperative Population)
  • Patient-centered Care
  • Clinical Outcomes
03

In context

Lead sponsor

SELDA MERT is the lead sponsor of 2 studies on the registry; 1 is 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

Inclusion criteria

  • Aged 65 years and older
  • Scheduled for elective surgery
  • Edmonton Frail Scale score ≥ 7
  • Able to speak Turkish and communicate effectively
  • Can be transferred from the postoperative intensive care unit to the ward
  • Patients who agree to participate in the study

Exclusion criteria

Exclusion Criteria:

  • Patients with neurological or psychological disorders
  • Patients who cannot be transferred from the postoperative intensive care unit to the ward
  • Emergency and unplanned cases
05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Investigator)
Enrollment
75 participants (estimated)

Study arms

  • No intervention
    Control group

    Standard nursing care was provided to patients in this group

  • Experimental
    Targeted Individualized Nursing Care Group

    An individualized nursing intervention targeting risk factors associated with frailty was planned for patients in this group

    Other: Experimental

Interventions

  • OtherExperimental

    Targeted Individualized Nursing Care

06

What researchers measure

Primary outcomes

  1. Cognitive Function - Standardized Mini-Mental State Examination (MMSE)

    Cognitive status will be assessed using the Standardized Mini-Mental State Examination (MMSE). The MMSE evaluates orientation, memory, attention, recall, language, and visuospatial skills. The total score ranges from 0 to 30, with higher scores indicating better cognitive function. Scores of 23 or below are generally considered indicative of cognitive impairment.

    Time frame: Postoperative day 1 and the day of discharge

  2. Cognitive Function - Delirium Risk - Nursing Delirium Screening Scale (Nu-DESC)

    Delirium risk will be evaluated using the Nursing Delirium Screening Scale (Nu-DESC). The scale assesses five domains: disorientation, inappropriate behavior, inappropriate communication, hallucinations, and psychomotor retardation. Each symptom is scored per shift as follows: 0 points: Symptom absent, 1 point: Symptom present/mild, 2 points: Symptom present and pronounced/severe A total score of 2 points or higher is considered indicative of delirium.

    Time frame: Postoperative day 1 and the day of discharge

  3. Physical Status Assessment - Pain Level - Numeric Rating Scale (NRS)

    Pain Level - Numeric Rating Scale (NRS): Pain intensity will be assessed using the Numeric Rating Scale (NRS). Patients rate their pain from 0 (no pain) to 10 (worst imaginable pain). Higher scores indicate greater pain intensity.

    Time frame: Postoperative day 1 and the day of discharge

  4. Physical Status Assessment - Katz Activities of Daily Living (ADL) Scale

    Katz Activities of Daily Living (ADL) Scale: Functional status will be evaluated using the Katz Activities of Daily Living (ADL) Scale, which assesses independence in six activities: bathing, dressing, toileting, transferring, continence, and feeding. Higher scores indicate greater independence in daily activities. Evaluation of the scale is based on the total score obtained from these items: 0-6 points: Dependent, 7-12 points: Partially dependent, 13-18 points: Independent.

    Time frame: Postoperative day 1 and the day of discharge

  5. Physical Status Assessment - Itaki Fall Risk Scale

    Itaki Fall Risk Scale: The Itaki Fall Risk Scale will be used to evaluate patients' risk of falling. The scale assesses various risk factors related to falls in hospitalized patients. The scale consists of 19 risk factors that may contribute to patient falls. The risk factors are categorized as major and minor, with 1 point assigned for each minor risk factor and 5 points for each major risk factor. Based on the total score obtained from evaluating all risk factors, two risk levels are defined: 0-4 points: Low risk, 5 points and above: High risk.

    Time frame: Postoperative day 1 and the day of discharge

  6. Nutritional Status - Mini Nutritional Assessment Short Form (MNA-SF)

    Mini Nutritional Assessment Short Form (MNA-SF): Nutritional status will be assessed using the Mini Nutritional Assessment-Short Form (MNA-SF). The total score ranges from 0 to 14, with higher scores indicating better nutritional status.

    Time frame: Postoperative day 1 and the day of discharge

  7. Psychological Status Assessment - Geriatric Depression Scale (GDS)

    Geriatric Depression Scale-15 (Short Form): It is a scale used to screen for depression in older adults. The total score ranges from 0 to 15. Scores of 0-4 indicate no depression, 5-8 indicate mild depression, 9-11 indicate moderate depression, and 12-15 indicate severe depression.

    Time frame: Postoperative day 1 and the day of discharge

07

Study locations

1 site
  • Eskişehir Osmangazi University Health, Practice, and Research Hospital
    Eskişehir, Turkey (Türkiye)
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 Apr 22, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07471945
Lead sponsor
SELDA MERT
Responsible party
SELDA MERT (PhD, Kirsehir Ahi Evran Universitesi) — Sponsor-investigator
First posted
Mar 13, 2026
Start date
Mar 1, 2026
Primary completion
Apr 30, 2026 (estimated)
Completion
Jun 30, 2026 (estimated)
Last update
Apr 22, 2026

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

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