The classic website will no longer be available as of June 25, 2024. Please use the modernized ClinicalTrials.gov.
Working…
ClinicalTrials.gov
ClinicalTrials.gov Menu

Effect of Augmented Low-dye* Taping and Exercise on Plantar Pressure, Navicular Drop and Foot Posture in Pes Planus (Ald)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT06034600
Recruitment Status : Active, not recruiting
First Posted : September 13, 2023
Last Update Posted : March 6, 2024
Sponsor:
Information provided by (Responsible Party):
Asli Oren, Inonu University

Brief Summary:

Introduction: Pes planus is a deformity that affects the foot-ankle muscle complex as well as passive components of the foot such as bones and ligaments. Various approaches such as taping methods and exercise training are being investigated in the treatment of pes planus. The effect of the applied methods and their superiority over each other are still unclear. The effect of banding methods varies according to the band type and technique. Exercise methods currently focus on the intrinsic and extrinsic muscles of the foot. Pedobarographic evaluations are also performed in addition to clinical evaluations to evaluate the effectiveness of treatments.

Objective: It is planned to compare the effects of reinforced low-dye taping method, which is one of the rigid taping techniques used in the treatment of pes planus, and exercise training on foot plantar pressure, navicular drop and foot posture.

Material and method: 34 individuals with pes planus between the ages of 18-25 will be included in the study, which was designed as a single-blind randomized study. The universe of our study will be Lokman Hekim University Faculty of Health Sciences and Institute of Health Sciences. The whole universe will be tried to be reached and individuals who meet the inclusion criteria will be selected from the relevant universe. Consent form will be obtained from individuals who are deemed eligible to participate in the study. Pes planus evaluation; It will be done using the navicular drop test and the foot posture index. In order for the physical activity levels of the groups to be homogeneous, after stratified sampling, individuals will be randomly assigned to the exercise groups by taping and exercise with the closed envelope method. Evaluations will be made to each group at the beginning, at the eighth and twelfth week. Static evaluation of the foot will be made using navicular drop and foot posture index, and pedobarographic analysis will be done using a foot analyzer.

Conclusion: The effects of taping and exercise training on foot static and plantar pressure measurements will be interpreted.


Condition or disease Intervention/treatment Phase
Pes Planus Other: taping Other: exercise Not Applicable

Detailed Description:
For taping application, intermittent taping will be done by the same researcher on the foot with pes planus three times a week. The applied hard taping technique will be applied continuously for eight weeks. The group that will perform exercises together with the taping treatment will perform the exercises with the resistance band without taping and then do the other exercises after the taping application. The applied taping will remain on the skin as long as it can until the next taping day. Individuals will be asked to note the length of stay of the tape on the skin. The exercises will be done three days a week for eight weeks. After verbal information about the research protocol to be applied, practical training will be given for the exercises. In the banding application, reinforced low-dye (ALD) technique, one of the hard banding techniques, will be applied. A hard tape will be used on the individuals by the same researcher throughout the study. With the tape application, to the participants; Information will be given about physical activity, shoes and issues that should be considered in daily life.

Layout table for study information
Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 34 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Intervention Model Description: Experimental, single-blind randomized controlled trial
Masking: Single (Participant)
Primary Purpose: Treatment
Official Title: Effect of Augmented Low-dye Taping and Exercise on Plantar Pressure, Navicular Drop and Foot Posture in Pes Planus
Actual Study Start Date : October 6, 2023
Estimated Primary Completion Date : April 15, 2024
Estimated Study Completion Date : September 1, 2024

Resource links provided by the National Library of Medicine


Arm Intervention/treatment
Experimental: exercise and taping
Individuals in this group are planned to practice exercise together with taping therapy for eight weeks.
Other: taping
Taping will be applied to the exercise and taping group after the exercises with theraband. Other exercises that are not performed will be performed with the tape on the skin.The application will be repeated three days a week for eight weeks.

Other: exercise
Stretching and strengthening exercises will be applied to both groups three days a week for 8 weeks.The exercises performed with theraband will be performed in the same way in both groups. While the other exercises will be done after taping in the "taping and exercise group", the "exercise group" will be done without taping.

Experimental: exercise
Individuals in this group are planned to receive only exercise practice for eight weeks.
Other: exercise
Stretching and strengthening exercises will be applied to both groups three days a week for 8 weeks.The exercises performed with theraband will be performed in the same way in both groups. While the other exercises will be done after taping in the "taping and exercise group", the "exercise group" will be done without taping.




Primary Outcome Measures :
  1. foot plantar pressure [ Time Frame: baseline, at 8 and 12 weeks ]
    A foot analyzer will be used in the pedobarographic evaluation of the foot.


Secondary Outcome Measures :
  1. navicular drop [ Time Frame: baseline, at 8 and 12 weeks ]
    The distance measurement from the ground with the navicular will be measured using the caliper. Three measurements will be taken and the average recorded.

  2. foot posture index [ Time Frame: baseline, at 8 and 12 weeks ]
    Each criterion is scored on a scale ranging from -2 to +2, when the score is between 0 and 5, the foot will be considered neutral and between 6 and +12 as pronation.



Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Layout table for eligibility information
Ages Eligible for Study:   18 Years to 25 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Be between the ages of 18-25
  • Navicular drop (ND) test >10 mm
  • Foot posture index ≥6
  • Individuals in the 1st and 2nd category according to the international physical activity survey
  • Individuals who volunteered to participate in the study

Exclusion Criteria:

  • Presence of systemic, neurological, rheumatological or orthopedic problems that may affect the lower extremity
  • Individuals who are allergic to the tape to be used
  • Individuals who cannot adapt to exercise or taping practices
  • Individuals who have received treatment for pes planus in the last 6 months
  • Individuals with a BMI ≥ 30
  • Presence of pregnancy
  • Cases not wanting to take part in the study

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT06034600


Locations
Layout table for location information
Turkey
Inonu Univercity
Malatya, Turkey
Sponsors and Collaborators
Inonu University
Investigators
Layout table for investigator information
Study Director: Burcu Talu, PhD Inonu University
Publications of Results:
Layout table for additonal information
Responsible Party: Asli Oren, Principal Investigator, Inonu University
ClinicalTrials.gov Identifier: NCT06034600    
Other Study ID Numbers: 2022/4027
0000-0002-5941-1619 ( Other Identifier: Orcid )
First Posted: September 13, 2023    Key Record Dates
Last Update Posted: March 6, 2024
Last Verified: March 2024
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

Layout table for additional information
Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Keywords provided by Asli Oren, Inonu University:
exercise
flat foot
Augmented Low-dye
navicular drop
plantar pressure
Additional relevant MeSH terms:
Layout table for MeSH terms
Flatfoot
Talipes
Foot Deformities, Acquired
Foot Deformities
Musculoskeletal Diseases
Foot Deformities, Congenital
Lower Extremity Deformities, Congenital
Limb Deformities, Congenital
Musculoskeletal Abnormalities
Congenital Abnormalities