Metatarsophalangeal Joint Sprain Kinesiotaping

Sponsor
Qassim University (Other)
Overall Status
Completed
CT.gov ID
NCT05982431
Collaborator
Cairo University (Other), Prince Sattam Bin Abdulaziz University (Other)
60
2
3
16.2
30
1.9

Study Details

Study Description

Brief Summary

kinesio taping would reduce pain, improve gait performance, and enhance the functional capacity of turf toe patients undergoing physical therapy

Condition or Disease Intervention/Treatment Phase
  • Other: Traditional physical therapy program
  • Other: Kinsio taping
  • Other: placebo Kinsio taping
N/A

Detailed Description

Health practitioners have recently become interested in using kinesiology taping in clinical practice as an alternative to traditional taping and bracing procedures for treating a variety of diseases, including sprain of metatarsophalangeal joint of the big toe. Patients with turf toe can benefit from kinesiology tape because it offers therapeutic support and stability while preserving a normal range of motion.

Study Design

Study Type:
Interventional
Actual Enrollment :
60 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Kinesiology Taping Helps Patients With First Metatarsophalangeal Joint Sprain
Actual Study Start Date :
Sep 10, 2021
Actual Primary Completion Date :
Aug 22, 2022
Actual Study Completion Date :
Jan 15, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: exercise group

60-minutes exercise program, three times a week on alternate days for 12 successive weeks.

Other: Traditional physical therapy program
60-minutes exercise program, three times a week on alternate days for 12 successive weeks
Other Names:
  • exercise program
  • Experimental: placebo kinesiology taping plus exercise group

    Kinesiology taping was used, however the strain was zero. Before each exercise session, the tape was changed every two days while the patients were present.

    Other: Traditional physical therapy program
    60-minutes exercise program, three times a week on alternate days for 12 successive weeks
    Other Names:
  • exercise program
  • Other: placebo Kinsio taping
    One full strip of kinesiology taping tape and one half-length strip were needed for the placebo kinesiology taping application
    Other Names:
  • placebo kinesiology taping
  • Experimental: kinesiology taping plus exercise group

    putting no stress on the opposite end and a 50% stretch from the top of the big toe to the heel along the back of the heel. After applying a 50% stretch from the top of the big toe to the second horizontal little strip between the big toe and second toe, place the ends below the toe diagonally with no stress.

    Other: Traditional physical therapy program
    60-minutes exercise program, three times a week on alternate days for 12 successive weeks
    Other Names:
  • exercise program
  • Other: Kinsio taping
    One full strip of kinesiology taping tape and one half-length strip were needed for the kinesiology taping application
    Other Names:
  • kinesiology taping
  • Outcome Measures

    Primary Outcome Measures

    1. Pain visual analog scale [at first week]

      The degree of the pain was assessed using a 10-cm visual analog scale (VAS), with 0 denoting no pain and 10 denoting the most painful event.

    2. Pain visual analog scale [after 12 weeks]

      The degree of the pain was assessed using a 10-cm visual analog scale (VAS), with 0 denoting no pain and 10 denoting the most painful event.

    3. Gait parameters (step length by centimeter). [at first week]

      The twelve computerized cameras of the VICON 3D motion analysis system were used to record gait data.

    4. Gait parameters (step length by centimeter). [after 12 weeks]

      The twelve computerized cameras of the VICON 3D motion analysis system were used to record gait data.

    5. Gait parameters (stride length by meter). [at first week]

      The twelve computerized cameras of the VICON 3D motion analysis system were used to record gait data.

    6. Gait parameters (stride length by meter). [after 12 weeks]

      The twelve computerized cameras of the VICON 3D motion analysis system were used to record gait data.

    7. Gait parameters (cadence by steps per minute). [at first week]

      The twelve computerized cameras of the VICON 3D motion analysis system were used to record gait data.

    8. Gait parameters (cadence by steps per minute). [after 12 weeks]

      The twelve computerized cameras of the VICON 3D motion analysis system were used to record gait data.

    9. Gait parameters (velocity by centimeter per second). [at first week]

      The twelve computerized cameras of the VICON 3D motion analysis system were used to record gait data.

    10. Gait parameters (velocity by centimeter per second). [after 12 weeks]

      The twelve computerized cameras of the VICON 3D motion analysis system were used to record gait data.

    Secondary Outcome Measures

    1. Functional ability assessment [at first week]

      Functional ability was assessed using the 6-minute walk test.

    2. Functional ability assessment [after 12 weeks]

      Functional ability was assessed using the 6-minute walk test.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    25 Years to 30 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • comprised athletes with 2nd grade turf toe.

    • medically stable.

    • had foot pain for more than a month prior to enrollment.

    • didn't have persistent, incapacitating pain.

    • had a doctor's note approving their decision to stop taking painkillers during the research.

    Exclusion Criteria:
    • if they had any surgical intervention before.

    • range of motion limitation in the ankle joint.

    • inability to exercise.

    • systemic disease.

    • any other orthopedic problem at ankle joints.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Outpatient Clinic of College of Applied Medical Sciences, Prince Sattam bin Abdulaziz University Al-Kharj Riyadh Saudi Arabia 11432
    2 King Khalid Hospital Al-Kharj Riyadh Saudi Arabia

    Sponsors and Collaborators

    • Qassim University
    • Cairo University
    • Prince Sattam Bin Abdulaziz University

    Investigators

    • Principal Investigator: Alshimaa Azab, PhD, Cairo University

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Maged Basha, Assistant Professor, College of Medical Rehabilitation, Qassim University, Qassim University
    ClinicalTrials.gov Identifier:
    NCT05982431
    Other Study ID Numbers:
    • RHPT/0021/0063
    First Posted:
    Aug 8, 2023
    Last Update Posted:
    Aug 8, 2023
    Last Verified:
    Aug 1, 2023
    Individual Participant Data (IPD) Sharing Statement:
    Yes
    Plan to Share IPD:
    Yes
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Maged Basha, Assistant Professor, College of Medical Rehabilitation, Qassim University, Qassim University
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Aug 8, 2023