Skip to content

Effects of Roy adaptation mode nursing on postoperative negative emotion and pain in patients with pancreatic cancer:A randomized controlled trial protocol

Effects of Roy adaptation mode nursing on postoperative negative emotion and pain in patients with pancreatic cancer:A randomized controlled trial protocol

Status
Unknown
Phases
Phase 1
Study type
Interventional
Source
TCTR
Registry ID
TCTR20220401004
Enrollment
66
Registered
2022-04-01
Start date
2022-06-15
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Pancreatic cancer is one of the most malignant tumors with high recurrence rate and poor prognosis. Surgical resection is an important treatment for pancreatic cancer. Compared with other benign diseases, pancreatic cancer patients will bear more psychological burden, postoperative pain, fatigue, dyspepsia, etc., seriously affecting the quality of life of patients. Postoperative negative emotions and pain care is very important for these patients. In recent years, domestic and foreign scholars h

Interventions

1.Physiological function adaptation: There will be obvious pain after pancreatic cancer surgery, so patients should be instructed to exercise deep breathing correctly to relax their mind
use phone to play interesting music or videos as a distraction
avoid behaviors that may cause or aggravate pain, and instruct the patient to take a comfortable position to avoid drainage obstruction caused by protrusion, compression, or distortion of the drainage
Experimental Other
Roy adaptation mode nursing on the basis of routine nursing.

Sponsors

Min Zhang
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1.Patients who has taken analgesic drugs for a long time. 2.Patients complicated with serious mental illness or disturbance of consciousness. 3.Patients suffering from negative emotions and pain caused by other serious diseases. 4.Patients who are unable to understand the study protocol or unwilling participants after explanation.

Exclusion criteria

Exclusion criteria: 1.Patients who have serious adverse events and are not suitable for the next step. 2.Patients whose disease progresses in the course of treatment and needs to change the treatment plan. 3.Patients with poor compliance, affecting effectiveness and safety judgment. 4.Patients who ask to leave the study for any reason.

Design outcomes

Primary

MeasureTime frame
Pain 5 weeks visual analogue scale (VAS),Negative emotion 5 weeks self-rating anxiety scale (SAS) and self- rating depression scale (SDS)

Secondary

MeasureTime frame
Quality of life scale 5 weeks World Health Organization quality of life scale-100, WHOQOL-100)

Countries

China

Contacts

Public ContactZhang Min

Ruijin Hospital affiliated to Shanghai Jiao Tong University School of Medicine

zm20507@rjh.com.cn18920586133

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026