NCT01761864

Brief Summary

Osteoarthritis is a common problem in primary care. Long-term use of non-steroidal anti-inflammatory drugs (NSAIDs) for pain relief can lead to serious (gastro-intestinal, cardiovascular and renal) adverse events, that can even result in death. NSAIDs differ in their risk of side effects. Opoid analgesics are sometimes used as an alternative for NSAIDs in patients with osteoarthritis. However, these drugs also can lead to serious adverse events. Simple analgesics are first line treatment in patients with osteoarthritis. NSAIDs and opoid analgesics should be avoided whenever possible. Farmaka (www.farmaka.be) is a non-profit organisation that operates a nationwide academic detailing service in Belgium since 2006. The academic detailing exists of face-to-face educational visits to general practitioners in their practice by a trained visitor with a medical science degree. The aim of these visits is to improve the quality of drug prescribing in primary care. Small scale experiments in the past showed that academic detailing can indeed improve prescribing behavior. The current study wants to examine if nationwide academic detailing on appropriate prescribing of analgesics for chronic pain in osteoarthritis results in a better GP's prescribing behavior. Another research question is whether physician-visitors have more influence on prescribing than non-physician visitors. It is also interesting to examine if the effect of a visit is larger if there exists a longstanding relationship between the academic detailer and the GP. About 4.000 general practices are located in a region where academic detailers of Farmaka are operational and have received a visit at least once before. All these practices will be divided into two study groups in a random manner. The first group of practices will belong to the treatment group. GP's from this group will be offered a face-to-face visit on appropriate prescribing of analgesics for chronic pain in osteoarthritis. The visits will take place between February and June 2013. The second group of practices will serve as a control group. GP's from these practices won't be offered any visit at all during the year 2013. Reimbursement data for all GP's are available by request from the Belgian Intermutualistic Agency (IMA). IMA data for 2013 will be available by the end of 2014. These data will allow comparison between the treatment and control group on the amound and type of prescriptions for analgesics in patients with chronic osteoarthritis pain. A comparison of the prescriptions of practices that participate in the study and the prescriptions of in practices that don't participate is also possible. The project is funded by the Federal Agency for Medicines and Health Products. We hypothesize that

  • the academic detailing visits to GP practices on prescribing of analgesics for chronic pain in osteoarthritis will improve prescribing of analgesics by at least 5%
  • the personal relation between the GP and the academic detailer, expressed as the number of previous visits, is an important effect modifier

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
4,000

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Feb 2013

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

January 2, 2013

Completed
5 days until next milestone

First Posted

Study publicly available on registry

January 7, 2013

Completed
25 days until next milestone

Study Start

First participant enrolled

February 1, 2013

Completed
2.9 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 1, 2016

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

January 1, 2016

Completed
Last Updated

October 1, 2021

Status Verified

September 1, 2021

Enrollment Period

2.9 years

First QC Date

January 2, 2013

Last Update Submit

September 28, 2021

Conditions

Outcome Measures

Primary Outcomes (1)

  • recommended prescribing of analgetics

    Short-term (1 month), intermediate (6 months) and long-term (\<= 1 year) use of * paracetamol, ibuprofen , naproxen, oxicams, coxibs, nabumeton, tramadol, tilidine; * recommended NSAIDs among those treated with NSAIDs expressed as percentage; * PPI among those treated with NSAIDs expressed as percentage in insured individuals over 60 years of age and their relevant subgroups.

    1 year

Study Arms (2)

intervention group

EXPERIMENTAL

academic detailing receiver

Behavioral: academic detailing intervention

control group

NO INTERVENTION

not receiving an academic detailing intervention

Interventions

Also known as: academic detailing intervention on evidence-based prescribing of analgetics in chronic joint pain
intervention group

Eligibility Criteria

Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • Professionally active GPs of all Belgian primary care practices that have received a visit before by Farmaka and are located in the regions where academic detailers are currently active. No age or gender restrictions.

You may not qualify if:

  • GPs who are not professionally active (anymore) in a practice located in a region were an academic detailer operates in the period of the visits on analgesics; GP's who have never received an academic detailing visit before.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Antwerp

Wilrijk, 2610, Belgium

Location

Related Publications (1)

  • Bruyndonckx R, Verhoeven V, Anthierens S, Cornelis K, Ackaert K, Gielen B, Coenen S. The implementation of academic detailing and its effectiveness on appropriate prescribing of pain relief medication: a real-world cluster randomized trial in Belgian general practices. Implement Sci. 2018 Jan 10;13(1):6. doi: 10.1186/s13012-017-0703-8.

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
TRIPLE
Who Masked
PARTICIPANT, CARE PROVIDER, INVESTIGATOR
Purpose
SUPPORTIVE CARE
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
professor

Study Record Dates

First Submitted

January 2, 2013

First Posted

January 7, 2013

Study Start

February 1, 2013

Primary Completion

January 1, 2016

Study Completion

January 1, 2016

Last Updated

October 1, 2021

Record last verified: 2021-09

Locations