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WithdrawnNCT07413510Updated May 29, 2026

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

An interventional study of Precision Nursing and Conventional Clinical Nursing in Colorectal Cancer, sponsored by Jiangsu Cancer Institute & Hospital. Withdrawn at 1 site in China. Open to participants aged 18 Years to 80 Years. Per ClinicalTrials.gov, last updated 2026-05-29.

Sponsored by Jiangsu Cancer Institute & Hospital · Not applicable, Interventional, and Treatment

Why this study was withdrawn
The trial was withdrawn before participant enrollment; no subjects were recruited and no data were collected.
Phase
Not applicable
Study type
Interventional
Enrollment
0
Allocation
Randomized
Ages
18 Years to 80 Years
Sex
All
01

Study 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.

Read the 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.

02

Conditions studied

  • Colorectal Cancer

Keywords

  • Laparoscopic Surgery
  • Precision Nursing
  • Perioperative Outcomes
  • Randomized Controlled Trial
03

In context

Colorectal Neoplasms

5,599 studies on the registry are indexed under Colorectal Neoplasms; 1,459 are open to participants now.

Browse Colorectal Neoplasms studies →

Lead sponsor

Jiangsu Cancer Institute & Hospital is the lead sponsor of 40 studies on the registry; 21 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years to 80 Years
Sexes eligible
All
Accepts 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

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.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
0 participants (actual)

Study arms

  • Experimental
    Precision Nursing Group

    Participants in this arm receive 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).

    Behavioral: Precision Nursing

  • Active comparator
    Conventional Care Group

    Participants in this arm receive routine perioperative clinical nursing, including standard preoperative health education, basic intraoperative monitoring, and postoperative standard care without personalized interventions.

    Behavioral: Conventional Clinical Nursing

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.

06

What researchers measure

Primary outcomes

  1. Preoperative anxiety score

    Anxiety 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.

    Time frame: 1 day before surgery

07

Study locations

1 site
  • Jiangsu Cancer Hospital
    Nanjing, Jiangsu 210009, China
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 May 29, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07413510
Lead sponsor
Jiangsu Cancer Institute & Hospital
Responsible party
Mei Fang (Nurse-in-Charge, Jiangsu Cancer Institute & Hospital) — Principal investigator
First posted
Feb 17, 2026
Start date
May 1, 2026
Primary completion
May 1, 2026
Completion
May 1, 2026
Last update
May 29, 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 withdrawn, as verified in May 2026. You cannot join it, but the record below documents what was studied.

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