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Precision Nursing vs Conventional Care in Laparoscopic Colorectal Cancer Surgery: A Randomized Controlled Trial

Comparison of Perioperative Outcomes Between Precision Nursing and Conventional Care in Laparoscopic Colorectal Cancer Surgery: a Randomized Controlled Trial

Status
Withdrawn
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07413510
Enrollment
0
Registered
2026-02-17
Start date
2026-05-01
Completion date
2026-05-01
Last updated
2026-05-29

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

Conditions

Colorectal Cancer

Keywords

Laparoscopic Surgery, Precision Nursing, Perioperative Outcomes, Randomized Controlled Trial

Brief summary

This single-center randomized controlled trial compares the effects of precision nursing and conventional care in patients undergoing laparoscopic colorectal cancer surgery. Precision nursing includes personalized preoperative psychological counseling, intraoperative body temperature and position management, and postoperative targeted recovery guidance. Conventional care follows routine clinical nursing procedures. The study will assess differences in perioperative outcomes (such as anxiety, intraoperative hypothermia, postoperative nausea and vomiting, recovery time, and hospital stay) between the two groups, to provide evidence for optimizing nursing strategies for colorectal cancer surgery patients.

Detailed description

Study Background: Laparoscopic colorectal cancer surgery is a common treatment, but perioperative complications (e.g., hypothermia, nausea) and anxiety affect patient recovery. Precision nursing may improve these outcomes, but evidence from RCTs is limited. Study Design: A parallel-group randomized controlled trial. 90 eligible patients are randomly assigned (1:1) to the precision nursing group or conventional care group. Interventions: Precision Nursing Group: 1. Preoperative: 30-minute personalized psychological counseling + music therapy; 2. Intraoperative: Real-time body temperature monitoring (maintaining ≥36°C) + dynamic position optimization; 3. Postoperative: Individualized recovery guidance (early ambulation, dietary adjustment) based on patient condition. Conventional Care Group: Routine clinical nursing (preoperative health education, intraoperative basic monitoring, postoperative standard care). Outcome Measures: Primary: Preoperative anxiety score (SAQ), intraoperative hypothermia rate, postoperative nausea and vomiting (PONV) incidence, time to first flatus, length of hospital stay; Secondary: Postoperative complication rate, nursing satisfaction score. Statistical Analysis: Data are analyzed using SPSS 26.0. Continuous variables are compared with t-tests, categorical variables with chi-square tests. A p-value \<0.05 is considered statistically significant.

Interventions

BEHAVIORALPrecision Nursing

Personalized perioperative care including 30-minute preoperative psychological counseling, real-time intraoperative body temperature monitoring (maintaining ≥36°C), and postoperative individualized recovery guidance (early ambulation, dietary adjustment).

BEHAVIORALConventional Clinical Nursing

Routine perioperative clinical nursing, including standard preoperative education, basic monitoring, and standard postoperative care.

Sponsors

Jiangsu Cancer Institute & Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Patients diagnosed with colorectal cancer and scheduled for laparoscopic surgery. * Age 18 to 80 years old. * Able to understand and complete the study questionnaires. * Voluntarily agree to participate in this study and sign the informed consent form.

Exclusion criteria

* Severe cognitive impairment or mental illness. * Emergency surgery patients. * Severe cardiopulmonary, hepatic, or renal dysfunction. * Patients who cannot cooperate with perioperative nursing interventions. * Participation in other clinical trials that may affect this study.

Design outcomes

Primary

MeasureTime frameDescription
Preoperative anxiety score1 day before surgeryAnxiety level of participants is evaluated using a validated Self-Rating Anxiety Scale (SAS). The scale consists of 20 items, with total scores ranging from 20 to 80 points. A higher score indicates a more severe level of preoperative anxiety.

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 30, 2026