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The effect of perioperative pain neuroscience education management combined with pre-rehabilitation exercises on pain and recovery quality after laparoscopic colorectal surgery: an exploratory randomized controlled clinical trial

The effect of perioperative pain neuroscience education management combined with pre-rehabilitation exercises on pain and recovery quality after laparoscopic colorectal surgery: an exploratory randomized controlled clinical trial

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200058931
Enrollment
Unknown
Registered
2022-04-20
Start date
2022-05-01
Completion date
Unknown
Last updated
2024-01-28

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

Conditions

None listed

Interventions

Experimental group:Perioperative pain neuroscience education combined with preoperative pre-rehabilitation exercise
Control group:Routine multimode analgesia during perioperative period

Sponsors

The First Affiliated Hospital of Chongqing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18-65 years, no gender limit; 2. 30 kg/m^2 >= BMI > 18kg/m^2; 3. Receive general anesthesia (tracheal intubation, combined nerve block); 4. ASA grading ?-?; 5. Laparoscopic colorectal surgery for colorectal tumors; 6. Fully informed and signed informed consent.

Exclusion criteria

Exclusion criteria: 1. Respiratory and cardiac arrest occurred during the operation; 2. Patients with mental diseases; 3. Patients whose operation was canceled and did not cooperate with follow-up; 4. Suffering from mental or neurological diseases and unable to express their wishes correctly; 5. Pregnant, lactating patients or patients with pregnancy intention; 6. Patients who have participated in clinical trials of other drugs within the last 3 months; 7. Patients who cannot be extubed in PACU should be brought back to ICU for further treatment after surgery; 8. Patients with mobility disorders; 9. Patients with cardiopulmonary dysfunction (New York Heart Function Scale greater than Level 2 or six-minute walk test less than 400 meters); 10. Patients undergoing secondary operation; 11. Patients deemed unsuitable for inclusion by the investigators.

Design outcomes

Primary

MeasureTime frame
moderate-to-severe pain 24 hours after surgery in motion;

Secondary

MeasureTime frame
five - dimensional health scale (EQ-5D-5L) score;perioperative opioid dosage;pain catastrophizing scale;quality of sleep after surgery;satisfaction for analgesia;

Countries

China

Contacts

Public ContactPeng Lihua

The First Affiliated Hospital of Chongqing Medical University

plhcqmu@163.com+86 15823443968

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026