Study of Changes in the Feet With Pregnancy
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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: NCT01868074 |
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Recruitment Status :
Completed
First Posted : June 4, 2013
Results First Posted : August 2, 2016
Last Update Posted : August 2, 2016
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| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| Pregnancy | Device: Insole | Not Applicable |
Show detailed description
| Study Type : | Interventional (Clinical Trial) |
| Actual Enrollment : | 72 participants |
| Allocation: | Randomized |
| Intervention Model: | Parallel Assignment |
| Masking: | Single (Outcomes Assessor) |
| Primary Purpose: | Treatment |
| Official Title: | Enhancing Women's Health Through Assessing Foot Plasticity With Pregnancy |
| Study Start Date : | May 2013 |
| Actual Primary Completion Date : | September 2013 |
| Actual Study Completion Date : | June 2014 |
| Arm | Intervention/treatment |
|---|---|
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No Intervention: Usual
Participants who are not randomized to the fitted insole intervention
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Experimental: Insole
Participants randomized to use of a custom-molded insole during pregnancy
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Device: Insole
Custom-molded arch-supporting insole |
- Change in Arch Drop [ Time Frame: baseline, 8 weeks postpartum ]Measurement of Arch Drop (Sitting arch height minus standing arch height) using Arch Height Index Measurement System
- Change in Arch Rigidity [ Time Frame: baseline, 8 weeks postpartum ]The arch rigidity index, a measure of the ability of the foot to maintain the arch when weight-bearing, was determined by dividing the standing AHI by the seated AHI. A value of 1.0 would indicate a perfectly rigid arch, while smaller values would indicate a more flexible arch.
- Change in CPEI (3mph) [ Time Frame: baseline, 8 weeks postpartum ]The Center of Pressure Excursion Index (CPEI) is a measurement of the lateral displacement of the center of pressure curve from a reference line drawn from the initial to the final centers of pressure during stance phase of gait, and standardized to the width of the anterior third of the foot during pedobarography.
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| Ages Eligible for Study: | 18 Years to 40 Years (Adult) |
| Sexes Eligible for Study: | Female |
| Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
- Women in their first trimester of pregnancy
- Ages 18 and 40
Exclusion Criteria:
- lower limb joint or spinal surgery
- inflammatory joint or muscle problems such as rheumatoid or psoriatic arthritis
- diabetes
- collagen disorder such as Marfan Syndrome, Ehlers-Danlos Syndrome, Mixed Connective Tissue Disease, or Osteogenesis Imperfecta
- cannot walk without any assistance
- surgeries or have another medical condition that may affect their walking ability
- flat feet (absence of a longitudinal arch)
- inability to return for the follow-up visit 2 months after delivery
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): NCT01868074
| United States, Iowa | |
| University of Iowa | |
| Iowa City, Iowa, United States, 52242 | |
| Principal Investigator: | Neil A Segal, MD | University of Iowa |
| Responsible Party: | Neil A Segal, Associate Professor, University of Iowa |
| ClinicalTrials.gov Identifier: | NCT01868074 |
| Other Study ID Numbers: |
201209787 |
| First Posted: | June 4, 2013 Key Record Dates |
| Results First Posted: | August 2, 2016 |
| Last Update Posted: | August 2, 2016 |
| Last Verified: | June 2016 |
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pregnancy, arch height, collapsed arch |

