Pro-self Pain Management in Norway

Not Applicable

Completed

• Conditions: Cancer; Pain
• Interventions: Behavioral: Pro self pain control programme

• Registration Number: NCT00760305
• Lead Sponsor: Oslo University Hospital

Brief Summary

The main aim of this study is to evaluate whether a patient education programme on cancer pain management compared to standard care decreases pain and increases patients quality of life. The investigators hypothesis is that patients and family caregivers who receive the intervention will have improved outcomes. Patients and family members are seen in their homes by the nurses doing the intervention over 6 weeks. Patients keep a diary of their pain and medication intake.

Detailed Description

The undertreatment of cancer pain remains a significant clinical problem. The PRO-SELF Pain Control Program is a 6 week psychoeducational intervention that was shown to improve pain management in oncology outpatients with pain from bone metastasis. However, this promising intervention requires replication in samples of oncology patients with cancer pain outside of the United States.

The purpose of the study was to test the effectiveness of The PRO-SELF Pain Control Program in Norwegian cancer patients and their family caregivers. Only data on patient outcomes will be presented.

The theoretical framework for this study incorporated elements of Orem's self-care theory, as well as the principles of academic detailing and nurse coaching to change patients' self-care behaviors regarding cancer pain management.

Two hundred adult cancer patients with pain from skeletal metastasis and their caregivers participated in this study. Patients were randomized to either the PRO-SELF program or standard care. Patients completed questionnaires about pain, physical functioning, quality of life, anxiety, and depression at the time of enrollment and after 6 weeks. Data on analgesics were collected through chart reviews and patient diaries. Both groups received home visits and telephone calls by an oncology nurse over a period of six weeks. Participants in the intervention group received education about pain management and were coached to improve their pain management behaviors. Two-way repeated measures analyses of variance will be done to determine differences in pain intensity scores and to evaluate the differences over time in the total amount of opioid analgesics taken by the patients.

Study Timeline

• Study Start: 2004-10
• Primary Completion: 2008-04
• Study Completion: 2008-04
• Status Verified: 2008-09
• Study First Submitted: 2008-09-25
• Study First Submitted QC: 2008-09-25
• Study First Posted: 2008-09-26
• Last Update Submitted: 2011-05-23
• Last Update Posted: 2011-05-24

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 167

Inclusion Criteria

• Greater than 18 years of age
• Radiographic evidence of bone metastasis
• Able to read and write Norwegian
• Average pain intensity of greater than 2.5

Exclusion Criteria

• Brain metastasis

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
1	Pro self pain control programme	Patients who received the Pro-Self psychoeducational intervention

Primary Outcome Measures

Name	Time	Method
Worst pain intensity	6 weeks

Secondary Outcome Measures

Name	Time	Method
Knowledge of cancer pain management	6 weeks

Trial Locations

Locations (1)

Ulleval University Hospital; 🇳🇴 Oslo, Norway