- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03507907
The Effects of Mulligan Mobilization Technique in Older Adults With Neck Pain
April 16, 2018 updated by: Caner Karartı, Hacettepe University
The Effects of Mulligan Mobilization Technique in Older Adults With Neck Pain: A Randomized Controlled, Double-Blind Study
When the literature is examined, there is study investigating the effect of mulligan mobilization technique on older adults with neck pain.
This study aims to investigate the effect of mulligan mobilization technique on pain, range of motion, functional level, kinesiophobia, fear of movement, depression and quality of life in older adults with neck pain.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Neck pain is common in older adults.
There are a lot of approaches for treatment of neck pain such as soft tıssue mobilizations, electirical stimulations etc. Mulligan proposes mobilization with movement (MWM) technique for various musculoskeletal disorders.
But there is no study related MWM for older adults with neck pain.
The purpose of this study is to examine the effect of mulligan mobilization technique on pain, range of motion (ROM), functional level, kinesiophobia, depression and quality of life (QoL) in older adults with neck pain.
The hypothesis of our study is MWM can be effective on ROM, kinesiophobia, depression and QoL in older adults with neck pain.
Study Type
Interventional
Enrollment (Actual)
40
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
-
-
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Kırşehir, Turkey, 40100
- Ahi Evran University
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-
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
65 years and older (OLDER_ADULT)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Ongoing neck pain for at least 3 months,
- Having no neurological, rheumatological or musculoskeletal problems
- Having not taken any analgesic medication for neck pain for the last 3 months.
Exclusion Criteria:
- Neck pain originating from various pathologies
- Presence of cord compression,
- Vertebrobasilar artery insufficiency,
- Severe radiculopathy,
- Osteoporosis or osteopenia (t score>-1),
- Long-term use of anticoagulant or corticosteroid drugs,
- Patients who had received any treatment for their neck pain.
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: TREATMENT
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: DOUBLE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
EXPERIMENTAL: Study Group
Mulligan mobilization techniques were applied to the older adults.
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Mulligan Mobilization techniques were applied to the older adults who included in study group.
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|
OTHER: Control Group
Conventional physiotherapy programs were applied to the older adults who included in control group.
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Conventional therapy was applied to the older adults who included in control group.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Visual Analogue Scale
Time Frame: 5 months
|
The severity of pain at rest and during activity was assessed by Visual Analogue Scale (VAS).
Participants were questioned about their average pain over the last 4 weeks.
They were asked to mark the severity of their pain on a 10-cm-long line where 0 represented no pain, and 10 stood for vicious pain
|
5 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Neck Disability Index
Time Frame: 5 months
|
This scale was used to evaluate how the participants' daily life was influenced by their neck pain.
Total score of the scale ranges from 0 to 35 and higher scores indicate higher levels of disability
|
5 months
|
|
Tampa Scale of Kinesiophobia
Time Frame: 5 months
|
This scale was used to assess the patients' fear of pain or re-injury due to movement.
It consists of 17 items and assesses various factors of fear/avoidance and injury/re-injury in several activities.
Total score of the scale varies between 17 and 68 and higher scores represent higher levels of kinesiophobia.
|
5 months
|
|
Universal goniometer
Time Frame: 5 months
|
A universal goniometer was used to assess the range of motion (ROM) of the cervical vertebrae.
Cervical flexion, extension, right and left lateral flexion and right and left rotation movements were measured 3 times in active manner while the patients were in a comfortable sitting position.
The average value of the measurements was recorded as ROM.
|
5 months
|
|
Beck Depression Inventory
Time Frame: 5 months
|
Participants' level of depression was assessed using this scale that consists of 21 categories with 4 options in each.
Each item has a score between 0 and 3 and total score varies from 0 to 63. Score ranges are interpreted as: 0-9 points = Minor depression, 10-16 points = Mild depression, 17-29 points = Moderate depression, and 30-63 points = Severe depression
|
5 months
|
|
Short Form-36
Time Frame: 5 months
|
This form was used to assess the quality of life (QoL) of the participants.
This questionnaire is consisted of 36 questions that are categorized into 8 groups as following: physical role functioning, emotional role functioning, bodily pain, energy, social role functioning, mental health, and general health perception.
Each category is scored on a 0-100 range, and higher scores indicate better QoL
|
5 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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)
May 20, 2017
Primary Completion (ACTUAL)
September 15, 2017
Study Completion (ACTUAL)
October 14, 2017
Study Registration Dates
First Submitted
April 10, 2018
First Submitted That Met QC Criteria
April 16, 2018
First Posted (ACTUAL)
April 25, 2018
Study Record Updates
Last Update Posted (ACTUAL)
April 25, 2018
Last Update Submitted That Met QC Criteria
April 16, 2018
Last Verified
April 1, 2018
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2018300
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
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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