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CompletedNCT07081113Updated Jun 30, 2026

Study Comparing Cyriax Mobilization and Muscle Energy Techniques for Improving Arm Function in People Recovering From Surgery for Distal Radius (Wrist) Fractures

An interventional study of Cyriax Mobilization and Muscle Energy Technique (MET) in Distal Radius Fracture Fixation and Stiffness of Hand, Not Elsewhere Classified, sponsored by University of Lahore. Completed at 1 site in Pakistan. Open to participants aged 18 Years to 40 Years. Per ClinicalTrials.gov, last updated 2026-06-30.

Sponsored by University of Lahore · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
76
Allocation
Randomized
Ages
18 Years to 40 Years
Sex
All
01

Study summary

This study aims to compare the effects of Cyriax Mobilization and Muscle Energy Techniques (METs) on functional recovery in patients who have undergone surgical fixation of distal radius fractures. A total of 76 participants between 18 and 40 years old will be randomly assigned to two groups. One group will receive Cyriax Mobilization with conventional therapy, while the other will receive METs with conventional therapy. Treatment will last four weeks with three sessions per week. Researchers will measure grip strength, pain levels, range of motion, and functional ability using standard assessment tools. The goal is to determine which therapy is more effective in improving hand and wrist function after surgery.

02

Conditions studied

  • Distal Radius Fracture Fixation
  • Stiffness of Hand, Not Elsewhere Classified
03

In context

Lead sponsor

University of Lahore is the lead sponsor of 223 studies on the registry; 40 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 40 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Patients aged 18 to 40 years.
  • Both male and female participants.
  • Patients in the post-operative phase (4-5 weeks after distal radius fracture fixation).
  • Patients with post-operative wrist stiffness and limited range of motion.

Exclusion criteria

Exclusion Criteria:

  • Open wounds at the fracture site or other fracture complications.
  • History of previous fracture in the same limb.
  • Comorbid conditions affecting hand function (e.g., rheumatoid arthritis).
  • Neurological deficits (e.g., wrist drop, carpal tunnel syndrome) Pregnancy
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
76 participants (actual)

Study arms

  • Experimental
    Group A - Cyriax Mobilization

    Participants in this group will receive Cyriax Mobilization along with conventional physical therapy and radiocarpal mobilization.

    Other: Cyriax Mobilization

  • Experimental
    Group B - Muscle Energy Techniques (METs)

    Participants in this group will receive Muscle Energy Techniques (reciprocal inhibition method) along with conventional physical therapy and radiocarpal mobilization.

    Other: Muscle Energy Technique (MET)

Interventions

  • OtherCyriax Mobilization

    Deep transverse friction massage applied to the wrist and forearm muscles, 3 sessions/week for 4 weeks, along with TENS and hot packs.

  • OtherMuscle Energy Technique (MET)

    Isometric contractions performed against therapist resistance to improve range of motion and reduce pain, 3 sessions/week for 4 weeks.

06

What researchers measure

Primary outcomes

  1. Pain intensity

    pain intensity, was measured using the Visual Analogue Scale (VAS, 0-10), with 0 denoting no pain and 10 denoting the most severe pain.

    Time frame: Baseline, Week 2, Week 4

Secondary outcomes

  1. grip strength

    measured using dynamometer.

    Time frame: baseline, week 2, week 4.

  2. functional disability

    functional disability assessed with the Disabilities of the Arm, Shoulder, and Hand (DASH) questionnaire (0-100).

    Time frame: baseline, week 2, week 4.

  3. ROM

    wrist range of motion (ROM) comprising flexion, extension, radial deviation, ulnar deviation, pronation, and supination measured with a standard goniometer (degrees)

    Time frame: baseline, week 2, week 4.

07

Study locations

1 site
  • University of Lahore
    Lahore, Punjab Province, Pakistan
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 30, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07081113
Lead sponsor
University of Lahore
Responsible party
Sponsor
First posted
Jul 23, 2025
Start date
Sep 1, 2025
Primary completion
Sep 30, 2025
Completion
Sep 30, 2025
Last update
Jun 30, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Mar 2025. You cannot join it, but the record below documents what was studied.

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