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CompletedNCT05258162METUpdated Feb 28, 2022

Comparison of Mobilization and MET Post-Traumatic Elbow Stiffness

An interventional study of Mobilization and Muscle Energy Technique in Elbow Fracture, sponsored by Riphah International University. Completed at 1 site in Pakistan. Open to participants aged 18 Years to 35 Years. Per ClinicalTrials.gov, last updated 2022-02-28.

Sponsored by Riphah International University · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 1 year 1 month after the study started (first participant enrolled Jan 2021, registered Feb 2022).
Phase
Not applicable
Study type
Interventional
Enrollment
30
Allocation
Randomized
Ages
18 Years to 35 Years
Sex
All
01

Study summary

The purpose of this study is to find the effects of Mobilization and Muscle energy technique in patients with post-traumatic elbow stiffness.

Read the detailed description

A randomized control trial was conducted at Benazir Bhutto Hospital, Rawalpindi. The sample size with reference to parent article was 10 calculated through open epi tool. But 30 patients were included in the study to increase the statistical power of analysis. The participants were divided into two interventional groups i.e. Group A and Group B, each having 15 participants. The study duration was 1 year. Sampling Technique applied was non probability purposive sampling technique. Random Allocation will be through sealed envelope method into two treatment group i.e. Group A and Group B. Only 18-35 years old patients (both male and female) with Post-traumatic elbow stiffness were included in the study. Tools that were used in the study are NPRS, DASH questionnaire, TAMPA scale and Goniometer. Total duration of treatment for both groups was 3 weeks, 3 days a week. Pre and post assessment was done. Data was analyzed through SPSS version 23.

02

Conditions studied

  • Elbow Fracture

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Keywords

  • Post Traumatic Elbow Stiffness
  • Pain
  • Elbow
  • Disability
  • Fracture
03

In context

Elbow Fractures

44 studies on the registry are indexed under Elbow Fractures; 13 are open to participants now.

This study's enrollment of 30 is below the median of 52 across 29 interventional studies indexed under Elbow Fractures.

Browse Elbow Fractures studies →

Lead sponsor

Riphah International University is the lead sponsor of 2,133 studies on the registry; 633 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years to 35 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Patients with post-operative elbow stiffness after distal end extra-articular humerus fractures.
  • Patients with proximal radius ulna fractures.
  • Minimum immobilization period of 3 weeks

Exclusion criteria

Exclusion Criteria:

  • Any ligament injury
  • Patients with Diabetes
  • Patients with RA
  • Patients with Pathological fractures
  • Revision surgeries
  • Neuro-vascular disorders.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
30 participants (actual)

Study arms

  • Experimental
    Mobilization

    Mobilizations are performed with minimum 6 seconds distraction stretch followed by partial release then followed by slow intermittent stretch at 3-4 seconds intervals. Oscillations for 2 minutes at 2-3 oscillations per second.

    Other: Mobilization

  • Experimental
    Muscle Energy Technique

    Muscle Energy Technique is given in the form of post isometric relaxation with 5-7 sec hold for 8-10 repetitions followed by a gentle passive stretch. Only 20% resistance is offered to the isometric contraction.

    Other: Muscle Energy Technique

Interventions

  • OtherMobilization

    Hot pack for ten minutes. Active and active-assisted exercises for the: * Elbow flexion and extension * Wrist flexion and extension * Forearm supination and pronation * Lock and key exercises. * Shoulder flexion, extension, abduction, adduction, and rotation (10 repetitions x 1sets) Low-intensity isometric resistance exercises for; * Elbow flexion and extension * Forearm supination and pronation (10 sec hold) (10 repetitions x 1 set) Resistance will be provided manually by the therapist. Along all these exercises Mobilisations are performed with minimum 6 seconds distraction stretch followed by partial release then followed by slow intermittent stretch at 3-4 seconds intervals. 3 days per week for 3 weeks. Oscillations for 2 minutes at 2-3 oscillations per second.

    Also known as: Hot pack, Range of Motion Exercises, Isometrics

  • OtherMuscle Energy Technique

    Hot pack for ten minutes. Active and active-assisted exercises for the: * Elbow flexion and extension * Wrist flexion and extension * Forearm supination and pronation * Lock and key exercises. * Shoulder flexion, extension, abduction, adduction, and rotation (10 repetitions x 1sets) Low-intensity isometric resistance exercises for; * Elbow flexion and extension * Forearm supination and pronation (10 sec hold) (10 repetitions x 1 set) Resistance will be provided manually by the therapist. Along all these exercises Muscle Energy Technique is given in the form of post isometric relaxation with 5-7 sec hold for 8-10 repetitions followed by a gentle passive stretch. Only 20% resistance is offered to the isometric contraction. 3 days per week for 3 weeks.

    Also known as: Hot pack, Range of Motion Exercises, Isometrics

06

What researchers measure

Primary outcomes

  1. Numeric pain rating scale

    Changes from baseline Numeric pain rating scale is a self-administered, or analyst reported, measuring instrument comprising of a scale that shows numerical ranges usually from 0-10 or 0-100. In this scale extreme or farthest point shows having 'no pain' to having 'extreme pain'.

    Time frame: 3rd week

  2. ROM Elbow (Flexion)

    Changes from baseline range of motion( ROM) of elbow joint flexion is taken by using Goniometer.

    Time frame: 3rd week

  3. ROM Elbow (Extension)

    Changes from baseline range of motion( ROM) of elbow joint extension is taken by using Goniometer.

    Time frame: 3rd week

  4. ROM Forearm (Supination)

    Changes from baseline range of motion( ROM) of forearm supination is taken by using Goniometer.

    Time frame: 3rd week

  5. ROM Forearm (Pronation)

    Changes from baseline range of motion (ROM) of forearm pronation is taken by using Goniometer.

    Time frame: 3rd week

Secondary outcomes

  1. Disability

    Changes from baseline disability is measured through DASH (Disability of the arm, shoulder and hand) questionnaire. DASH questionnaire is a self reported area specific outcome measuring tool for symptoms and disabilities in upper limb. It mainly comprise of a 30-items scale which is further consist of questions related to difficulty in performing normal daily activities, scored on 5 response options. Scores for these 30 items then calculate on a scale of 0 (no disability) to 100 (most severe disability)

    Time frame: 3rd week

  2. kinesiophobia (fear of movement)

    Changes from baseline kinesiophobia is measured through Tampa scale which is a 17 item scale. Total scores of this scale ranges from 17-68. Where 17 means no kinesiophobia and 68 means severe kinesiophobia while score of ± 37 indicates that there is kinesiophobia.

    Time frame: 3rd week

07

Study locations

1 site
  • Benazir Bhutto Hospital
    Rawalpindi, Punjab 46300, Pakistan
08

References and documents

Individual participant data

Plan to share: No

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 Feb 28, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05258162
Lead sponsor
Riphah International University
Responsible party
Sponsor
First posted
Feb 28, 2022
Start date
Jan 18, 2021
Primary completion
Jan 30, 2022
Completion
Jan 30, 2022
Last update
Feb 28, 2022

Study contacts

Muhammad Affan Iqbal, PhD*
principal investigator · Riphah International University

Oversight

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

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