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

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01595035
Enrollment
200
Registered
2012-05-09
Start date
2012-05-31
Completion date
2021-02-28
Last updated
2021-03-02

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

Conditions

Postoperative Pain, Chronic Pain

Keywords

Day surgery, Orthopedic surgery, Breast reconstruction surgery

Brief summary

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.

Interventions

Patients randomized to the intervention group will receive written information about pain and pain treatment in a booklet before surgery and contacted by telephone 24, 48, 72 hours and 7 days after surgery to be coached in pain management

Sponsors

Oslo University Hospital
CollaboratorOTHER
Helse Stavanger HF
CollaboratorOTHER_GOV
Oslo Metropolitan University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Average pain intensity1 weekBrief Pain Inventory

Secondary

MeasureTime frameDescription
The relationships between pain sensitivity, catastrophizing, perceived barriers to pain management and adherence to analgesics and pain intensity.1,2,3,7 day after surgery
Pain occurence3 and 6 month after surgeryBrief Pain Inventory

Countries

Norway

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 16, 2026