Rotator Cuff DiseaseNCT00624117
Progressive Exercise After Operation of Rotator Cuff Rupture and Anterior Labrum Rupture
A study testing Progressive exercise in people with Rotator Cuff Disease and Shoulder Joint, run by Jyväskylä Central Hospital at 1 site in Finland.
Trial summary
The purpose of this study is to evaluate the effectiveness of progressive strength training after rotator cuff and labrum operation of the shoulder joint. Read more about this study
- Who is it for?
- Ages 18 to 65 years
- Conditions the study is for
- Rotator Cuff Disease, Shoulder Joint
- What is being tested?
- Progressive exercise
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 100 participants
- Where
- 1 siteFinland
- Study dates
- May 2006to Feb 2010
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 65 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- rupture of rotator cuff
- rupture of anterior labrum
- age 18 to 65 years
- motivated to continue in work life
- motivated for rehabilitation
Who cannot join
- former operation in the same joint
- major arthrosis in the same joint
- cervical disk herniation
- concised spinal cord
- conditions after cervical spine operations
- rheumatic diseases
Show all 12Show fewer
- fibromyalgia
- pregnancy
- severe depression
- alcoholism
- misusing of drugs
- disease that prevents progressive exercise eg. back pain, heart disease
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Progressive Exercise After Operation of Rotator Cuff Rupture and Anterior Labrum Rupture: Randomized Controlled Trial
The purpose of this study is to evaluate the effectiveness of progressive strength training after rotator cuff and labrum operation of the shoulder joint.
- Conditions
- Rotator Cuff Disease, Shoulder Joint
- Being tested
- Progressive exercise
- Keywords
- shoulder joint, recovery of function, effectiveness of rehabilitation, rehabilitation
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Progressive exerciseBehavioural
home-based exercise program, 2 to 3 exercise sessions per week
| Study group | Role | What they receive |
|---|---|---|
| A | Experimental | Not described Receives: Behavioral: Progressive exercise |
What is being measured
The primary outcome is the main question the study is designed to answer.
Strength and mobility
Measured: one year
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted26 Feb 2008 (estimated)
- Study startMay 2006
- Primary completionFeb 2009
- Study completionFeb 2010
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Rotator Cuff DiseaseStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind
- Who is masked
- Outcomes assessor
- Enrolment
- 100 participants (actual)
Sponsor and investigators
- Lead sponsor
- Jyväskylä Central Hospital
- Sponsor type
- University, hospital or other
- Investigators
- Jari Ylinen, PhD, Principal investigator, Jyväskylä Central Hospital
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT00624117
- Sponsor's protocol ID
- Dnro46/2005
- Status last verified
- May 2010
- First submitted
- 15 Feb 2008
- Last updated
- 27 May 2010
- Results posted
- No
- Data monitoring committee
- No
Study at a glance
From the registry record, last updated by the sponsor on 27 May 2010. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Progressive Exercise After Operation of Rotator Cuff Rupture and Anterior Labrum Rupture: Randomized Controlled Trial
- ClinicalTrials.gov ID
- NCT00624117
- Acronym / sponsor ID
- Dnro46/2005
- Conditions
- Rotator Cuff Disease, Shoulder Joint
- Keywords
- shoulder joint, recovery of function, effectiveness of rehabilitation, rehabilitation
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 100 participants (actual)
- Lead sponsor
- Jyväskylä Central HospitalUniversity, hospital or other
- Study start
- May 2006
- Primary completion
- Feb 2009 (actual)
- Study completion
- Feb 2010 (actual)
- First posted
- 26 Feb 2008 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The purpose of this study is to evaluate the effectiveness of progressive strength training after rotator cuff and labrum operation of the shoulder joint.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (outcomes assessor)
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| A | Experimental | Behavioral: Progressive exercise |
Who may qualify
- Ages
- 18 to 65 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (5 listed)
- rupture of rotator cuff
- rupture of anterior labrum
- age 18 to 65 years
- motivated to continue in work life
- motivated for rehabilitation
Key exclusion criteria (12 listed)
- former operation in the same joint
- major arthrosis in the same joint
- cervical disk herniation
- concised spinal cord
- conditions after cervical spine operations
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Progressive exercisehome-based exercise program, 2 to 3 exercise sessions per week | Behavioural | A |
Primary outcome
Strength and mobility
Time frame: one year
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 27 May 2010.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Jari Ylinen, PhD principal investigator
Jyväskylä Central Hospital
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Progressive exercise in people with Rotator Cuff Disease and Shoulder Joint, run by Jyväskylä Central Hospital at 1 site in Finland.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 5 inclusion and 12 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 27 May 2010. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Finland. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Strength and mobility (time frame: one year). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 27 May 2010; AzTrials last refreshed its copy on 7 Nov 2026.