- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02020772
Coordinating Teams in Primary Health Care.
October 19, 2021 updated by: Norwegian University of Science and Technology
Coordination Between General Practitioners and Physical Therapists in Primary Health Care for Musculoskeletal Pain: Effect on Sick Leave and Referral to Specialist Care.
Patients who suffer from musculoskeletal pain often have more than one diagnosis.
These patients mostly have to wait a long time for the doctor's examination and treatment, and they also often have a sick leave for a long period of time.
The investigators expect that treatment and follow-up by an coordinating interdisciplinary team can improve these patients opportunity to function, increase their quality of life, and decrease their pain.
The purpose of this study is to investigate if use of a coordinating interdisciplinary team in primary health care will result in reduced sick leave compared with practice as usual, and give fewer referrals to specialized health services and private rehabilitation centers.
Research data will be obtained from the patients journals, questionnaires, and clinical examinations..
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
969
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Stjørdal, Norway
- Stjørdal Legesenter
-
Trondheim, Norway
- Persaunet Legesenter
-
Trondheim, Norway
- Rosten legesenter
-
Trondheim, Norway
- Sjøsiden Legesenter
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
21 years to 58 years (ADULT)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- patient in one of the participating general practices
- musculoskeletal complaints in 3 years before start of this study
- informed consent
Exclusion Criteria:
-
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: HEALTH_SERVICES_RESEARCH
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: SINGLE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
EXPERIMENTAL: coordinating primary health care 1
musculoskeletal pain care by a coordinating team of one general practitioner and two physical therapists
|
|
|
ACTIVE_COMPARATOR: usual primary health care 1
usual care of musculoskeletal pain in general practice
|
|
|
EXPERIMENTAL: coordinating primary health care 2
musculoskeletal pain care by a coordinating team of one general practitioner and two physical therapists
|
|
|
ACTIVE_COMPARATOR: usual primary health care 2
usual care of musculoskeletal pain in general practice
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
change in sick leave
Time Frame: 3 years
|
average number of days sick leave during 3 years pre-intervention and during the first, second and third year of the study
|
3 years
|
|
referrals to specialist care
Time Frame: 3 years
|
number of referrals to specialist care including private rehabilitation centers
|
3 years
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Study Director: Siv Mørkved, prof phd, Norwegian University of Science and Technology
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (ACTUAL)
December 1, 2013
Primary Completion (ACTUAL)
August 1, 2018
Study Completion (ACTUAL)
August 1, 2018
Study Registration Dates
First Submitted
December 19, 2013
First Submitted That Met QC Criteria
December 19, 2013
First Posted (ESTIMATE)
December 25, 2013
Study Record Updates
Last Update Posted (ACTUAL)
October 27, 2021
Last Update Submitted That Met QC Criteria
October 19, 2021
Last Verified
October 1, 2021
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2012/1232
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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