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Educational Intervention Targeting Nurses Attitudes and Knowledge About Cancer-related Pain Management

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT01313234
First Posted: March 11, 2011
Last Update Posted: January 8, 2013
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
Blekinge Institute of Technology
  Purpose
The purpose of this study is to investigate whether an intervention consisting of the implementation of guidelines about daily systematic pain assessment following a theory based education, targeting cancer-related pain and pain treatment, lead to a significantly positive improvement in RNs knowledge of, and attitudes towards their pain management. Furthermore will the interventions targeting the RNs influence the admitted patient's perception of their cancer-related pain?

Condition Intervention
Neoplasms Behavioral: Education

Study Type: Interventional
Study Design: Allocation: Non-Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Health Services Research
Official Title: A Theory Based Educational Intervention Targeting Nurses Attitudes and Knowledge Concerning Cancer-related Pain Management: A Study Protocol of a Quasi-experimental Study Design

Further study details as provided by Blekinge Institute of Technology:

Primary Outcome Measures:
  • Change from baseline of the total score of Knowledge and Attitudes Survey Regarding Pain [ Time Frame: Measurement will occur at first session of the educational intervention and 2 and 6 weeks after ]
    Nurses attitude and knowledge as measured by a modified version of the instrument: Knowledge and Attitudes Survey Regarding Pain


Secondary Outcome Measures:
  • Change from Baseline - Brief Pain Inventory, Short Form (BPI-SF) [ Time Frame: Measurement will occur at admission of the patient and at discharge from the hospital. Estimated average time period from admission to discharge is 2 weeks ]
    BPI-SF is a pain-assessment instrument developed for cancer patient. The instrument consists of nine items, and a figure depicting a human body where the patient marks position and type of pain. BPI-SF includes items concerning the degree of pain right now, pain during the last day and pain on average as well as items concerning effect of pain treatment, walking ability, mood, work, relationships and if sleep are affected by pain.


Enrollment: 60
Study Start Date: April 2011
Study Completion Date: December 2011
Primary Completion Date: June 2011 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: Education
Educational theory based intervention and systematic daily pain assessment
Behavioral: Education
Theory based education and systematic daily assessment
No Intervention: Control
Control group with care as usual

  Eligibility

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Cancer diagnosis
  • Aged 18 years and above
  • Cognitively intact and able to verbally communicate
  • At admission pain intensity >1 on Visual Analogue Scale (VAS)

Exclusion Criteria:

  • Trauma or planned and/or acute surgery.
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01313234


Locations
Sweden
Blekinge Hospital
Karlskrona, Sweden, 37185
Sponsors and Collaborators
Blekinge Institute of Technology
  More Information

Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
Responsible Party: Blekinge Institute of Technology
ClinicalTrials.gov Identifier: NCT01313234     History of Changes
Other Study ID Numbers: BFR20100046019
First Submitted: March 5, 2011
First Posted: March 11, 2011
Last Update Posted: January 8, 2013
Last Verified: January 2013

Additional relevant MeSH terms:
Cancer Pain
Pain
Neurologic Manifestations
Nervous System Diseases
Signs and Symptoms