Taping Technique With Supervised Exercises Protocol on Pain and Functional Status in Individuals With Arthritis

NCT ID: NCT04589871

Last Updated: 2020-10-20

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

40 participants

Study Classification

INTERVENTIONAL

Study Start Date

2019-06-05

Study Completion Date

2019-12-19

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

Osteoarthritis (OA) is claimed to be a global burden and a key health issue that affects the large weight-bearing joints of the lower extremity such as the knee and hip joints. The study was aimed to find out the efficacy of the tapping technique in addition to the supervised exercise protocol on pain intensity and functional status of an individual with patella-femoral arthritis.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

The study was based on a controlled pretest-posttest experimental group design. After initial screening, forty individuals (mean age 55years, ranged 40-60years) with patello-femoral arthritis randomly (n=20each) assigned into two group A and B. Group A received taping technique in addition to the supervised exercises protocol while group B received supervised exercises protocol only. Both the groups received their specified treatment 5 consecutive days in a week for 4weeks. Data collected for the variables (VAS and WOMAC) at day1 pre-intervention (baseline) and at day 28th post-intervention. The t-test used for within and between group analysis with keeping the p\<0.05.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Patellofemoral Osteoarthritis

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Two-arm parallel groups randomized control trial
Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Participants Outcome Assessors

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Group A

Group A received a taping technique in addition to the supervised exercises protocol

Group Type EXPERIMENTAL

Taping technique

Intervention Type OTHER

Fixmull stretch and Leukotape (rigid tape) were used in taping to guide the patellar trajectory orientation while performing the movement. Individuals were asked to lay down in supine position with knee in a slightly bent position. Fixomull stretch was used as an adhesive pre-wrap to protect the skin and provide some of the checking force. The main check strap was provided by stripes of rigid tape (Leukotape). The knee cap was taped, started on the outer aspect of the knee cap and pulled inwards. Finished at the back of the inside of the knee. Two further pieces of tape (Fixomull Stretch and Leukotape) applied distal to the patella unloaded the infrapatellar fat pad.

A supervised exercise protocol

Intervention Type OTHER

Quadriceps Strengthening; Terminal knee extension; Ball kicking; Strengthening of Vastus Medialis;

Group B

Group B received supervised exercises protocol only

Group Type ACTIVE_COMPARATOR

A supervised exercise protocol

Intervention Type OTHER

Quadriceps Strengthening; Terminal knee extension; Ball kicking; Strengthening of Vastus Medialis;

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Taping technique

Fixmull stretch and Leukotape (rigid tape) were used in taping to guide the patellar trajectory orientation while performing the movement. Individuals were asked to lay down in supine position with knee in a slightly bent position. Fixomull stretch was used as an adhesive pre-wrap to protect the skin and provide some of the checking force. The main check strap was provided by stripes of rigid tape (Leukotape). The knee cap was taped, started on the outer aspect of the knee cap and pulled inwards. Finished at the back of the inside of the knee. Two further pieces of tape (Fixomull Stretch and Leukotape) applied distal to the patella unloaded the infrapatellar fat pad.

Intervention Type OTHER

A supervised exercise protocol

Quadriceps Strengthening; Terminal knee extension; Ball kicking; Strengthening of Vastus Medialis;

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* The individuals with unilateral patella-femoral osteoarthritis
* Aged between 40-60years;
* Pain more than 3cm on VAS;
* Crepitus on movement,
* Showing osteophytes on standing skyline view of radiograph (Kallgren/Lawrence grade ≄2),
* found positive for the special tests (coordination test for the muscle vastus medialis, apprehension test for patellar, Clarke's test, and Waldron's test with phase I and II)

Exclusion Criteria

* The individuals with involvement of tibio-femoral joint;
* Presence of patella alta/baja;
* History of rheumatoid arthritis/traumatic knee, knee surgeries within six months
* On steroid injection, neurological deficit, fragile skin around the knee, allergic to tape;
* Poor cooperation
Minimum Eligible Age

40 Years

Maximum Eligible Age

60 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

King Saud University

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

AMIR IQBAL

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

AMIR IQBAL, MPT-Ortho

Role: PRINCIPAL_INVESTIGATOR

Rehabilitation Research Chair, CAMS, King Saud University, Riyadh, Saudi Arabia

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Rehabilitation Research Chair

Riyadh, , Saudi Arabia

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Saudi Arabia

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

RRC-2019-16

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.