Mulligan Mobilization With Arm Movement in CTS Patients
The Effect of the Mulligan Spinal Mobilization Technique With Arm Movement on Pain, Grip Strength, and Functionality in Individuals With Carpal Tunnel Syndrome
2 other identifiers
interventional
30
1 country
1
Brief Summary
The aim of this study was to investigate the effect of the Mulligan Spinal Mobilization with Arm Movement technique on pain, grip strength and functionality in individuals with carpal tunnel syndrome and to compare it with the conventional neurodynamic mobilization technique. The study aims to answer the following questions: Is the Mulligan spinal mobilization technique with arm movement superior to the conventional neurodynamic mobilization technique in terms of pain, grip strength, and functionality in individuals with carpal tunnel syndrome? Does the Mulligan spinal mobilization technique with arm movement outperform the conventional neurodynamic mobilization technique in terms of pain, grip strength, and functionality in individuals with carpal tunnel syndrome? The evaluation process took place in three stages for both groups: Baseline (pre-test), 6 weeks after the start of the study (post-test), and 12 weeks after the start of the study (follow-up test).
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Jun 2023
1 active site
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
Study Start
First participant enrolled
June 1, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 15, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
January 10, 2025
CompletedFirst Submitted
Initial submission to the registry
June 20, 2025
CompletedFirst Posted
Study publicly available on registry
June 29, 2025
CompletedJuly 2, 2025
June 1, 2025
1.5 years
June 20, 2025
June 29, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Pain Intensity
Pain intensity was assessed using the Visual Analog Scale (VAS), ranging from 0 (no pain) to 10 (worst pain), at rest and during activity with higher scores indicating worse pain.
Baseline, 6th week, 12th week
Functional Status and Symptom Severity
Functional status and symptom severity were evaluated using the Boston Carpal Tunnel Questionnaire, including the Functional Status Scale (FSS) and Symptom Severity Scale (SSS). Each scale ranges from 1 to 5. Higher scores indicate greater disability (FSS) or more severe symptoms (SSS).
Baseline, 6th week, 12th week
Secondary Outcomes (4)
Hand Grip Strength
Baseline, 6th week, 12th week
Range of Motion of the Wrist
Baseline, 6th week, 12th week
Sensory Function
Baseline, 6th week, 12th week
Pain Quality - McGill Pain Questionnaire
Baseline, 6th week, 12th week
Study Arms (2)
Mulligan Spinal Mobilization with Arm Movement
EXPERIMENTALParticipants in this group received Mulligan spinal mobilization applied to the cervical spine at C5, C6, and C7 levels, in 3 sets of 3 repetitions per level. During mobilization, participants actively performed arm movements in a neurodynamic stretching position. The intervention was administered 3 sessions per week for 6 weeks. Additionally, all participants performed tendon gliding and hand strengthening exercises three times per week for 6 weeks, which were also prescribed as home-based programs.
Conventional Neurodynamic Mobilization
ACTIVE COMPARATORParticipants in this group received conventional neurodynamic mobilization techniques targeting the median nerve, applied by a therapist. The intervention was administered 3 sessions per week for 6 weeks, with 3 sets of 3 repetitions in each session. In addition, all participants performed tendon gliding exercises and hand strengthening exercises three times per week for 6 weeks. These exercises were also assigned as home-based programs.
Interventions
In the neurodynamic SNAGs technique, participants sat on a chair. The therapist placed the medial border of the distal phalanx of one thumb under the facet joints of the C5, C6, and C7 levels, respectively. Then, the therapist placed the tip of the other thumb on the lateral side of the first thumb. In neurodynamic spinal mobilization combined with arm movement, the therapist provided manual contact to the affected spinous process level by supporting the medial aspect of one thumb with the index finger of the other hand. The therapist applied a transverse shift from the affected side to the unaffected side, but only in the transverse plane. While the glide was in progress, the patient was asked to perform neurodynamic movements for the median nerve, including scapular depression, shoulder abduction, elbow extension, forearm supination, and wrist and finger extension, all without crossing the pain limit for the affected side.
A neurodynamic mobilization technique involving a specific sequence of movements along the median nerve line was applied. For the right side, the procedure was performed as follows: The individual was placed supine on a stretcher. The therapist stood on the right side of the stretcher, facing the participant, with their right leg in front of their left leg. The individual's arm rested on the therapist's right thigh, and the therapist held the individual's right hand with his left hand. During the procedure, the therapist placed one hand on the individual's shoulder to depress the shoulder girdle by pressing the scapula downward. The individual's shoulder was abducted 90° and laterally rotated, and the forearm was supinated. The wrist, thumb, and fingers were extended. In this position, the therapist dynamically alternated between simultaneous elbow flexion/wrist extension and simultaneous elbow extension/wrist flexion.
Tendon glide exercises were performed in five consecutive positions. Each position was practiced for seven seconds, with three sets of five repetitions and one minute of rest between sets. Participants were asked to perform the exercises three times during the day. Hand muscle strengthening exercises were performed by placing a tire on the fingertips, abducting the fingers, and stretching the tire to strengthen the intrinsic muscles and fingers. Resistance could be increased by thickening the tire or adding a second one. Participants were given a grip strength exercise. The hand grip exercise strengthened the extrinsic muscles. Finger flexion and extension exercises strengthened the hand and finger muscles. Participants were asked to perform 10 repetitions of each exercise in each session and to perform the strengthening exercises three times during the day.
Eligibility Criteria
You may qualify if:
- Having a diagnosis of mild to moderate carpal tunnel syndrome (CTS).
- Being between 20 and 60 years of age.
- Having symptoms of paresthesia, pain, and numbness in areas of the hand related to the median nerve lasting more than six weeks.
- A positive Tinel, Phalen, or carpal compression test during wrist examination.
You may not qualify if:
- Pregnancy.
- The patient has a contraindication to exercise.
- Additional neurological, rheumatological, and orthopedic conditions.
- A positive Spurling test.
- Patients who have undergone surgery in the wrist or neck region.
- Presence of a tumor or pathology in the cervical region.
- Patients who have received physical therapy for the wrist or neck in the last six months.
- The patient has mental health issues.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Beste Gebologlulead
Study Sites (1)
Istanbul Medipol University
Istanbul, Marmara, 34810, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Pınar KAYA SARIBAS, Assoc Prof
Istanbul Medipol University, Faculty of Health Sciences, Department of Physiotherapy and Rehabilitation
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- Physiotherapist and Graduate Student Researcher
Study Record Dates
First Submitted
June 20, 2025
First Posted
June 29, 2025
Study Start
June 1, 2023
Primary Completion
December 15, 2024
Study Completion
January 10, 2025
Last Updated
July 2, 2025
Record last verified: 2025-06
Data Sharing
- IPD Sharing
- Will not share
This is a non-commercial academic thesis study and there is no plan to share individual participant data (IPD) with other researchers.