The Effects of 12-week Custom-made Orthotic Intervention on the Structure and Function of the Foot of Healthy Young Adults During Gait Termination

NCT ID: NCT02957812

Last Updated: 2018-03-01

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 18 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2016-11-30
• Study Completion Date: 2017-08-31

Brief Summary

The purpose of this study is to explore the long-term effects that orthotics imposes on the structure and function of the foot. The objectives of the study are to determine if the use of custom-made foot orthotics (CFO) cause: (a) changes to the structure of the plantar intrinsic muscles, (b) changes in the rate of muscle activity and timing in the plantar intrinsic muscles and (c) creates any changes in balance control during gait termination. The aim of the study is to enhance the appropriate dispensing of orthotics, and whether additional measures, such as rehabilitation exercises are necessary to increase their overall effectiveness in the clinical setting.

Detailed Description

Between 20-30 healthy young adults of both males and females will be recruited. A screening questionnaire will be administered to ensure that participants are appropriate for the study.

Once the participant has met the criteria of the study, the participants will be randomly allocated into one of two groups: (a) the control group or (b) the intervention group. Individuals that are selected to be in the intervention group, will be fitted with custom-made orthotics by an experienced pedorthist. The pedorthist will cast the foot posture using a foam impression to custom the design of the foot orthotic. The participant will have a week to acclimatize to the new environment, and if any discomfort arises the pedorthist will make any necessary corrections and the participant will have another week to acclimatize to the orthotic. The control group will not receive an intervention and ask to go about their daily life activities. All participants will undergo the same testing procedures at 6 and 12 weeks after baseline testing.

At baseline, 6 weeks and 12 weeks post-baseline, the researcher will take a diagnostic ultrasound image of the foot muscles prior to the gait trials. The researcher will also place 12 infrared markers and surface electrodes on the participant. All trials will be performed barefoot. The participants will then undergo a gait termination protocol. Participants will walk down an 8m walk-way with three force plates are embedded into the ground. Participants will be asked to walk to the end of the platform until instructed to stop. For 20% of the gait trials, the participants are walking forward until they hear an audio buzzer sound that will signal them to terminate their gait suddenly in the next two steps. All trials will be randomized.

Conditions

Flatfoot

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: SUPPORTIVE_CARE
• Blinding Strategy: NONE

Study Groups

Orthotics

Custom made orthotic provided for study

Group Type: EXPERIMENTAL

Custom-made Foot Orthotics (CFO)

Intervention Type: DEVICE

Provides longitudinal arch support

Control

Wearing own footwear

Group Type: NO_INTERVENTION

No interventions assigned to this group

Interventions

Custom-made Foot Orthotics (CFO)

Provides longitudinal arch support

Intervention Type: DEVICE

Eligibility Criteria

Inclusion Criteria

• a score of (+5) on the Foot Posture Index (FPI)
• navicular height < 3.6cm
• able to walk

Exclusion Criteria

• have worn CFOs in the past year,
• current lower limb injury, leg or foot pain
• neurological or musculoskeletal disorders affecting the function of the foot
• previous history of lower limb surgery
• protein intake above the recommended daily allowance (RDA)
• medications that effect balance.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 35 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Wilfrid Laurier University

OTHER

Sponsor Role: lead

Responsible Party

Katrina Protopapas

Principal Investigator

Responsibility Role: PRINCIPAL_INVESTIGATOR

Locations

Biomechanics Lab

Waterloo, Ontario, Canada

Countries

Canada

Other Identifiers

5114

Identifier Type: -

Identifier Source: org_study_id