Study Stopped
The trial was withdrawn before participant enrollment; no subjects were recruited and no data were collected.
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
1 other identifier
interventional
N/A
1 country
1
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
Started May 2026
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
February 10, 2026
CompletedFirst Posted
Study publicly available on registry
February 17, 2026
CompletedStudy Start
First participant enrolled
May 1, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 1, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
May 1, 2026
CompletedMay 29, 2026
May 1, 2026
Same day
February 10, 2026
May 26, 2026
Conditions
Keywords
Outcome Measures
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.
1 day before surgery
Study Arms (2)
Precision Nursing Group
EXPERIMENTALParticipants 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).
Conventional Care Group
ACTIVE COMPARATORParticipants in this arm receive routine perioperative clinical nursing, including standard preoperative health education, basic intraoperative monitoring, and postoperative standard care without personalized interventions.
Interventions
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).
Routine perioperative clinical nursing, including standard preoperative education, basic monitoring, and standard postoperative care.
Eligibility Criteria
You may qualify if:
- 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.
You may not qualify if:
- 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.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Jiangsu Cancer Hospital
Nanjing, Jiangsu, 210009, China
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Nurse-in-Charge
Study Record Dates
First Submitted
February 10, 2026
First Posted
February 17, 2026
Study Start
May 1, 2026
Primary Completion
May 1, 2026
Study Completion
May 1, 2026
Last Updated
May 29, 2026
Record last verified: 2026-05
Data Sharing
- IPD Sharing
- Will not share