Mobilization With Movement Versus Joint-Specific Manipulation in De Quervain's Tenosynovitis
Comparative Study on the Effectiveness of Mobilization With Movement Versus Joint Specific Manipulation on Pain and Function in Patient With Dequervains Tenosynovitis
1 other identifier
interventional
32
1 country
1
Brief Summary
A comparative study on the effectiveness of mobilization with movement (MWM) versus joint-specific manipulation (JSM) in patients with De Quervain's tenosynovitis typically aims to assess how each technique impacts pain relief and functional improvement. De Quervain's tenosynovitis is an inflammation of the tendons around the thumb and wrist, often causing pain, swelling, and difficulty in performing everyday tasks. The study would likely compare the two interventions by measuring pain levels, range of motion, and overall functional outcomes before and after treatment. MWM involves applying specific, controlled movements while the patient is actively engaging in their joint motion, targeting the tissue's mobility and reducing pain. JSM, on the other hand, focuses on manipulating the joint directly to restore normal function, specifically targeting the wrist and thumb regions affected by the condition.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Feb 2025
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
February 17, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 17, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
February 17, 2025
CompletedFirst Submitted
Initial submission to the registry
February 20, 2025
CompletedFirst Posted
Study publicly available on registry
April 9, 2025
CompletedApril 25, 2025
April 1, 2025
Same day
February 20, 2025
April 24, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Pain Reduction - Measured using the Numeric Pain Rating Scale (NPRS) (0-10 scale).
Pain intensity will be assessed using the Numeric Pain Rating Scale (NPRS), a validated tool where participants rate their pain on a scale from 0 no pain to 10 worst possible pain.
6 Months
Secondary Outcomes (1)
Wrist Function - Assessed with the Patient-Rated Wrist Evaluation (PRWE) (0-100 scale).
6months
Other Outcomes (1)
Clinical Signs - Evaluated using Finkelstein's Test (Positive/Negative).
6 months
Study Arms (2)
Joint-specific Manipulation
EXPERIMENTALGroup A
Mobilization with Movement
PLACEBO COMPARATORGroup B
Interventions
Mobilization with Movement * The proximal row of carpals glides passively radially. * Active thumb and wrist movements superimposed on the glide. Therapeutic excercises: * Ball Toss * Static web gripping * Gentle ROM activities to maintain mobility * Isometric exercises in all direction
Joint Specific Manipulation * High-velocity, low-amplitude thrust to the first carpometacarpal joint * Radiocarpal wrist mobilization .Grade III-IV applied at end range. 2. Therapeutic excercises: * Ball Toss * Static web gripping * Gentle ROM activities to maintain mobility * Isometric exercises in all direction Ergonomics modifications
Eligibility Criteria
You may qualify if:
- Age between 25-45 years.
- Positive Finkelstein test.
- Pain over the first dorsal compartment.
- Limited wrist and thumb function.
- Willingness to take part and adhere to the study's guidelines.
You may not qualify if:
- Previous surgery of wrist or thumb.
- Presence of neurological symptoms like numbness, weakeness.
- Rheumatological conditions like rheumatoid arthritis.
- Pregnancy.
- Presence of wrist fracture or osteoporosis.
- Carpel tunnel syndrome.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Riphah international University Malakand Campus
Malakand, KPK, 23060, Pakistan
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Dr.Nadeem Ahmad, MS
Riphah International University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- PARTICIPANT
- Purpose
- HEALTH SERVICES RESEARCH
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
February 20, 2025
First Posted
April 9, 2025
Study Start
February 17, 2025
Primary Completion
February 17, 2025
Study Completion
February 17, 2025
Last Updated
April 25, 2025
Record last verified: 2025-04
Data Sharing
- IPD Sharing
- Will not share