NCT05356624

Brief Summary

this study will investigate the effects of mobilization with movement in addition to soft tissue mobilization on pain and range of motion in patients suffering from De Quervain Tenosynovitis.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
30

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Apr 2022

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
unknown

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

April 15, 2022

Completed
11 days until next milestone

First Submitted

Initial submission to the registry

April 26, 2022

Completed
6 days until next milestone

First Posted

Study publicly available on registry

May 2, 2022

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 15, 2022

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

September 15, 2022

Completed
Last Updated

May 2, 2022

Status Verified

April 1, 2022

Enrollment Period

4 months

First QC Date

April 26, 2022

Last Update Submit

April 26, 2022

Conditions

Keywords

de quervains tenosynovitispainmanual therapyROM

Outcome Measures

Primary Outcomes (2)

  • Visual analogue scale

    It is a 100 mm scale drawn on a paper to determine the level or intensity of pain in range of (0 to 10)

    3 months

  • Goniometry

    The science of measuring the joint ranges in each plane of the joint is called goniometry. Goniometer is a device that measures an angle or permits the rotation of an object to a definite position. Neck flexion, extension, side bending and rotation will be assessed

    3 months

Study Arms (2)

Mulligan Mobilization

EXPERIMENTAL

Mobilization with movement (3 sets per 10 repetitions).

Other: Mulligan Mobilization

Soft tissue mobilization

EXPERIMENTAL

Soft tissue mobilization (3 sets per 10 repetitions)

Other: Soft Tissue Mobilization

Interventions

It is technique in which passive mobilization is applied by therapist to improve the normal position and by holding the passive glide active movement in restricted direction of motion to reduce pain or improve range of motion or function. A total of 3 sets of 10 repetition three times a week on alternate days for 6 week

Mulligan Mobilization

in this technique for joint the passive glides are applied, for CMC joint mobilization patient hand is rest on table. The therapist grasp trapezium with one hand and 1st metacarpal between index and thumb of other hand to apply glide. A total of 3 sets of 10 repetition three times a week on alternate days for 6 weeks.

Soft tissue mobilization

Eligibility Criteria

Age20 Years - 50 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Male and female
  • to 50 years
  • Subjects with pain in base of thumb (9)
  • Subject with positive fienklstein test

You may not qualify if:

  • History of radiculopathy
  • History of systemic illness
  • History of connective tissue disorder
  • Rheumatoid arthritis
  • History of hand or wrist injury or acute trauma
  • Subject with negative fienklstein test

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Aziz Bhatti Shaheed hospital

Gujrat, Punjab Province, 38000, Pakistan

RECRUITING

MeSH Terms

Conditions

De Quervain DiseasePain

Condition Hierarchy (Ancestors)

Tendon EntrapmentTendinopathyMuscular DiseasesMusculoskeletal DiseasesNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • Nosheen Manzoor, MS-OMPT

    Riphah International University

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Nosheen Manzoor, MS-OMPT

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

April 26, 2022

First Posted

May 2, 2022

Study Start

April 15, 2022

Primary Completion

August 15, 2022

Study Completion

September 15, 2022

Last Updated

May 2, 2022

Record last verified: 2022-04

Data Sharing

IPD Sharing
Will not share

Locations