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Recruiting

NCT Number: NCT06686277

Effects Of Gong's Versus Mulligan Mobilization In Patients With Adhesive Capsulitis

A Randomized Clinical Trial will be conducted at DHQ hospital kasur,BIT hospital kasur,Arif memorial hospital Lahore.Pre-diagnosed patients will be reassessed by applying (Shoulder Shrug Sign, Hand to neck, Hand to scapula, Hand to opposite scapula,Hand to back,Capsular pattern movement restriction)Plus all other special tests will be applied to confirm that symptoms are not due to other shoulder pathologies but are due to just adhesive capsulitis then through consecutive sampling technique on 60 patients they will be allocated using computer generated sampling(random number table) into Group A and Group B.

Recruiting

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Key information

Age range

40 year–50 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Iffat Anwar Medical Complex

Lahore, Punjab Province, Pakistan

Location status: Recruiting

Location contact

Abid Hanif Awan, M.Phill PT

CONTACT

[email protected]

03039878088

Adeena Nisar, DPT

PRINCIPAL_INVESTIGATOR

About this study

A Randomized Clinical Trial will be conducted at DHQ hospital kasur,BIT hospital kasur,Arif memorial hospital Lahore.Pre-diagnosed patients will be reassessed by applying (Shoulder Shrug Sign, Hand to neck, Hand to scapula, Hand to opposite scapula,Hand to back,Capsular pattern movement restriction)Plus all other special tests will be applied to confirm that symptoms are not due to other shoulder pathologies but are due to just adhesive capsulitis then through consecutive sampling technique on 60 patients they will be allocated using computer generated sampling(random number table) into Group A and Group B. Group A will be treated with Gong's mobilization and Group B will be treated with Mulligan MWM The procedures will be performed Three sets of 10 repetitions, with 1 minute rest between sets,thrice per week for a total of six weeks. Pre and post intervention values will be taken on 1st day and after 6 weeks. Outcome measures will be conducted through VAS for pain,SPADI for functional disability , goniometer for range of motion ,SF-36 for quality of life after 6 weeks. Data will be analyzed during SPSS software version 25. After assessing normality of data by Shapiro-wilk test, it will be decided either parametric or non-parametric test will be used within a group or between two groups.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age 40 to 50 years
  • Both male and female
  • Pre-diagnosed Unilateral Primary Frozen shoulder patients
  • Prediagnosed Stage 3(Frozen phase) patients(27)

Exclusion criteria

  • Patients with previous surgery in the shoulder joint
  • History of recent fracture or severe trauma to the shoulder
  • Diagnosed instability or previous history of dislocation
  • Systemic inflammatory conditions(e.g.rheumatoid arthritis)

Treatment and study plan

Gong's Mobilization Technique

Other

The therapist will push the scapula of the affected side in a posterior to anterior direction with one hand, and pushed the humeral head in an anterior to posterior direction parallel to joint plane with the other hand.

mulligan mobilization technique

Other

Mulligan Mobilization Technique

Primary outcomes

  1. Level of Pain

    Time frame: Pre & Post 6 weeks

    Numeric Pain Rating Scale

  2. Range of Motion

    Time frame: Pre & Post 6 weeks

    Goniometer

  3. Functional Disability

    Time frame: Pre & Post 6 weeks

    Shoulder Pain and Disability Index

  4. Quality of Life Level

    Time frame: Pre & Post 6 weeks

    Sort Form Survey-36

Study contacts

Contact information is provided by the study sponsor or research team.

Imran Amjad, Phd PT

CONTACT

[email protected]

03324390125

Sponsors and collaborators

Lead sponsor

Riphah International University

Other

Registry information

Official study title

Effects Of Gong's Versus Mulligan Mobilization On Pain, Range Of Motion, Functional Disability and Quality Of Life In Patients With Adhesive Capsulitis

Important dates

Study start
2024
Primary completion
2025
Study completion
2025
First posted
Nov 13, 2024
Registry last updated
Nov 13, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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