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A Clinical Trial of a Psycho-educational Intervention to Improve Pain Management After Day Surgery

CompletedNot applicableNCT01595035
View the official record on ClinicalTrials.gov

Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.

This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.

Brief summary (from the registry)

Evidence indicates that postoperative pain after day surgery is inadequately controlled. Patients have different experiences and knowledge about how to deal with pain, and the need for information and clarification may vary. The aim of this study is to enhance pain management by academic detailing (patients' current knowledge and motivations are the basis for information) and nurse coaching (frequent and individualized support). The study consists of 4 phases; (1) a pilot study about patients experience with pain after surgery by a structured telephone interview; (2) development of an intervention to improve pain management; (3) implement and evaluate the intervention; (4) evaluate the incidence of chronic pain after day surgery. Even if patients are prescribed sufficient doses of analgesics, pain relief is dependent on patients' adherence with the analgesic regimen. Psychological factors, such as catastrophizing may also contribute to patients' experience of postoperative pain. Strategies that may be more effective than general information concerning surgery and pain management is academic detailing and nurse coaching, and will be used as frame for the intervention. Hypothesis: Over the seven days after surgery patients in the intervention group report; * higher adherence with the analgesic regimen, * have less pain intensity and pain interference with function and * lower severity of side effects compared to the control group.

Study details

Official title
A Randomized Clinical Trial of a Psycho-educational Intervention to Improve Pain Management After Day Surgery
Interventions
  • Behavioral: psychoeducational
Sponsor
Oslo Metropolitan University
Collaborators
Oslo University Hospital; Helse Stavanger HF
Start date
2012-05
Primary completion
2020-02
Sex
All
Age range
from 18 Years
Results posted
No results posted in this snapshot
Countries
Norway
Total sites listed
1

Eligibility criteria

Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * \> 18 years of age; * able, to read, write, and understand Norwegian; * are scheduled for orthopedic (shoulder, bunnies), or breast reconstruction surgery and * have a telephone line. Exclusion Criteria: * Staying overnight in hospital

Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT01595035