Shoulder Impingement SyndromeNCT05871944
Effectiveness of Kaltenborn End Range Joint Mobilization Technique and Post FacilitationStretch in Shoulder Impingement Syndrome
A study testing KAlternborn Joint Mobilization and Post stretch Facilitation Technique in people with Shoulder Impingement Syndrome, run by Neuro Counsel Hospital, Pakistan at 1 site in Pakistan.
Trial summary
This study is a experimental one to observe the efficacy of joint mobilization and post facilitation techniques in shoulder impingement syndrome Read more about this study
- Who is it for?
- Ages 25 to 45 yearsHealthy volunteers can take part
- Conditions the study is for
- Shoulder Impingement Syndrome
- What is being tested?
- KAlternborn Joint Mobilization and Post stretch Facilitation Technique
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 20 participants
- Where
- 1 sitePakistan
- Study dates
- 5 Jan 2023to 4 May 2023
- 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 25 to 45 years
- All sexes
- Healthy volunteers accepted
- Adult
Who may be able to join
- Both male and female
- Age 25 to 45
- Diagnosed Rotator cuff impingement from ortho, neuro and musculoskeletal department
- Hawkin kennedy test positive
- Neer's test positive
- Jobe's test positive
Who cannot join
- Cervical spine disorder
- Fractures
- Major upper limb surgery
- Tumor or wound
- Diagnosed acromial malformations
Trial locations and contacts
1 site in 1 country.
Pakistan1 site
Al Nafees Medical Hospital, Islamabd
Islamabad, Federal, 44000
About this study
Official title: Effectiveness of Kaltenborn End Range Joint Mobilization Technique and Post Facilitation Stretch in Shoulder Impingement Syndrome
This study is a experimental one to observe the efficacy of joint mobilization and post facilitation techniques in shoulder impingement syndrome
Read the detailed description
his study is a experimental one to observe the efficacy of Kalternborn end range joint mobilization and post facilitation techniques in shoulder impingement syndrome. Goniometer, shoulder disability index will be the tool used for evaluation
- Conditions
- Shoulder Impingement Syndrome
- Being tested
- KAlternborn Joint Mobilization, Post stretch Facilitation Technique
- Medical subject headings
- Shoulder Impingement Syndrome
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
KAlternborn Joint MobilizationOther
This is a join mobilization technique to reduce the joint stiffness and help in improving joint range of motion
Post stretch Facilitation TechniqueOther
This is a PNF techniques used to relax the muscles and help in getting more free range of restricted joint
| Study group | Role | What they receive |
|---|---|---|
| control group | Active comparator | kalternborn joint mobilization techniques will be administered for total of 8 weeks at the rate of 2 session per week. Receives: Other: KAlternborn Joint Mobilization |
| experimental group | Experimental | Post stretch facilitation technique will be administered for total of 8 weeks at the rate of 2 session per week. Receives: Other: Post stretch Facilitation Technique |
What is being measured
The primary outcome is the main question the study is designed to answer.
Goniometer
This is a instrument designed to evaluate the joint range of motion. Greater ranges mean more mobility of joint and less means more restriction
Measured: 4 weeks
Shoulder Pain and Disability Index
Used to assess the patients level of pain and the ADLs which are affected. O score means no dysfuction of joint and higer score means more dysfuction
Measured: 4 weeks
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted23 May 2023
- Study start5 Jan 2023
- Primary completion4 May 2023
- Study completion4 May 2023
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Shoulder Impingement SyndromeStudies 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
- Model description
- Two groups will be formed. one group will receive joint mobilization technique and other will get post facilitation stretch technique
- Masking
- Single blind
- Who is masked
- Participant
- Enrolment
- 20 participants (actual)
Sponsor and investigators
- Lead sponsor
- Neuro Counsel Hospital, Pakistan
- Sponsor type
- University, hospital or other
- Collaborators
- Al Nafees Medical Hospital, Islamabad, National Institute of Rehabilitation Medicine, Islamabad, Pakistan
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05871944
- Sponsor's protocol ID
- 341
- Status last verified
- May 2023
- First submitted
- 13 May 2023
- Last updated
- 23 May 2023
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided: Have not decided yet about this.
Study at a glance
From the registry record, last updated by the sponsor on 23 May 2023. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Effectiveness of Kaltenborn End Range Joint Mobilization Technique and Post Facilitation Stretch in Shoulder Impingement Syndrome
- ClinicalTrials.gov ID
- NCT05871944
- Acronym / sponsor ID
- 341
- Conditions
- Shoulder Impingement Syndrome
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 20 participants (actual)
- Lead sponsor
- Neuro Counsel Hospital, PakistanUniversity, hospital or other
- Collaborators
- Al Nafees Medical Hospital, Islamabad, National Institute of Rehabilitation Medicine, Islamabad, Pakistan
- Study start
- 5 Jan 2023 (actual)
- Primary completion
- 4 May 2023 (actual)
- Study completion
- 4 May 2023 (actual)
- First posted
- 23 May 2023 (actual)
- 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.
This study is a experimental one to observe the efficacy of joint mobilization and post facilitation techniques in shoulder impingement syndrome
Detailed description
his study is a experimental one to observe the efficacy of Kalternborn end range joint mobilization and post facilitation techniques in shoulder impingement syndrome. Goniometer, shoulder disability index will be the tool used for evaluation
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (participant)
- Number of arms
- 2
- Model description
- Two groups will be formed. one group will receive joint mobilization technique and other will get post facilitation stretch technique
| Arm | Type | Receives |
|---|---|---|
| control group | Active comparator | Other: KAlternborn Joint Mobilizationkalternborn joint mobilization techniques will be administered for total of 8 weeks at the rate of 2 session per week. |
| experimental group | Experimental | Other: Post stretch Facilitation TechniquePost stretch facilitation technique will be administered for total of 8 weeks at the rate of 2 session per week. |
Who may qualify
- Ages
- 25 to 45 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult
Key inclusion criteria (6 listed)
- Both male and female
- Age 25 to 45
- Diagnosed Rotator cuff impingement from ortho, neuro and musculoskeletal department
- Hawkin kennedy test positive
- Neer's test positive
Key exclusion criteria (5 listed)
- Cervical spine disorder
- Fractures
- Major upper limb surgery
- Tumor or wound
- Diagnosed acromial malformations
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 |
|---|---|---|
| KAlternborn Joint MobilizationThis is a join mobilization technique to reduce the joint stiffness and help in improving joint range of motion | Other | control group |
| Post stretch Facilitation TechniqueThis is a PNF techniques used to relax the muscles and help in getting more free range of restricted joint | Other | experimental group |
Primary outcome
Goniometer
Time frame: 4 weeks
This is a instrument designed to evaluate the joint range of motion. Greater ranges mean more mobility of joint and less means more restriction
Shoulder Pain and Disability Index
Time frame: 4 weeks
Used to assess the patients level of pain and the ADLs which are affected. O score means no dysfuction of joint and higer score means more dysfuction
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 23 May 2023.
- Individual participant dataSharing planned: Undecided. Have not decided yet about this.
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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.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing KAlternborn Joint Mobilization and Post stretch Facilitation Technique in people with Shoulder Impingement Syndrome, run by Neuro Counsel Hospital, Pakistan at 1 site in Pakistan.
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 6 inclusion and 5 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 23 May 2023. 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 Pakistan. 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?
Goniometer (time frame: 4 weeks). The study lists 2 primary outcomes in all. 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 23 May 2023; AzTrials last refreshed its copy on 6 Nov 2026.