Effplant: Effect of Stimulating Plant on the Balance in Young Healthy

Sponsor
University of Valencia (Other)
Overall Status
Completed
CT.gov ID
NCT02508766
Collaborator
(none)
184
2

Study Details

Study Description

Brief Summary

The primary purpose of this study was to examine the immediate effect of manual stimulation on the foot plant in static and dynamic balance in young healthy subjects. In addition, the secondary objectives of this study were: 1) to identify whether manual stimulation of the foot plant in healthy young subjects, carried out with an easily reproducible protocol with 10 minutes duration, improves static balance, measured with Unipedal Stance Test; 2) to assess whether, manual stimulation of the foot plant in healthy young subjects, carried out with an easily reproducible protocol with 10 minutes duration, improves dynamic balance test, measured with Star Excursion Balance Test.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Plantar stimulation
N/A

Detailed Description

Methods Participants Participants from the University of Valencia (Spain) were asked to volunteer to participate in this study. Patients were included if they were university students and were able and willing to complete the protocol. Participants were excluded if they were ≥40 years-old or had a known musculoskeletal lower extremity injury (eg, postoperative conditions, musculotendinous or ligamentous problems), previous history of neurological problems, balance disorders (eg, vestibular or visual problems) or did some type of physical activity programme where balance exercises were performed.

Study design We conducted a randomized single-blind controlled study investigation. A non-stratified randomization list was generated and held centrally in sealed envelopes. Therefore, participants were randomly assigned to an experimental group, who received a plantar stimulation on the right foot, or to a control group, which did not receive any intervention.

Intervention Plantar stimulation In addition, a plantar stimulation directed at the plantar surface of the dominant foot was performed by an experienced physiotherapist, as described below. Participants performed one practice trial of plantar stimulation prior to performance. The manipulation was performed with the subject in the supine position. The intervention lasted ten minutes and consisted of four stages: 5 glide pressures focused on each interdigital space and on the internal longitudinal arch of the foot in a caudal direction, that lasted 10 seconds in duration, (2) 5 compression-decompression of each metatarsophalangeal joint, until a slight tension was perceived by the researcher at the joint, (3) 5 glide pressures applied for 5 seconds each, on the region of metatarsal heads, and (4) 5 static pressures applied for 10 seconds each, focused on four points of the sole: the head of the first and the fifth metatarsal head, the heel and the medial side of the midfoot (Figure 3). Duration of pressures was assessed by using an on-line metronome. Furthermore, all pressures, both static and glide, were measured by a strength dynamometer and the mean force of pressure was 48N. After the stimulation, given to the negative effects of the sudden standing-up on several study results, participants stood quietly for 20 seconds before balance tests.

Study Design

Study Type:
Interventional
Actual Enrollment :
184 participants
Allocation:
Randomized
Intervention Model:
Factorial Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
EFFECT OF MANUAL PLANTAR STIMULATION ON STATIC AND DYNAMIC POSTURAL CONTROL IN YOUNG HEALTHY SUBJECTS
Study Start Date :
Jul 1, 2015
Actual Primary Completion Date :
Jul 1, 2015
Actual Study Completion Date :
Jul 1, 2015

Arms and Interventions

Arm Intervention/Treatment
Experimental: Plantar stimulation

The manipulation was performed with the subject in the supine position. The intervention lasted ten minutes and consisted of four stages: 5 glide pressures focused on each interdigital space, that lasted 10 seconds in duration, 5 compression-decompression of each metatarsophalangeal joint, 5 glide pressures applied for 5 seconds each, on the region of metatarsal heads, 5 static pressures applied for 10 seconds each, focused on four points of the sole.

Procedure: Plantar stimulation
The manipulation was performed with the subject in the supine position. The intervention lasted ten minutes and consisted of four stages: 5 glide pressures focused on each interdigital space, that lasted 10 seconds in duration, 5 compression-decompression of each metatarsophalangeal joint, 5 glide pressures applied for 5 seconds each, on the region of metatarsal heads, 5 static pressures applied for 10 seconds each, focused on four points of the sole.

No Intervention: Control group

Volunteers received no intervention. They just sat there for 20 minutes before being evaluated.

Outcome Measures

Primary Outcome Measures

  1. Anthropometric measurements (the measure is a composite) [1 day]

    Height (cm) Mass (kg). Body mass index was calculated from height and mass data (kg/m2). Bilateral leg length measures (cm). On a plinth with participant in supine, leg length was assessed using a standard tape measure. The distance between the anterior superior iliac spine and the most distal portion of the medial malleolus of the same leg was measured. Both legs were evaluated.

Secondary Outcome Measures

  1. Static postural control testing: Unipedal Stance Test [1 day]

    Static balance was assessed using the UPST. Firstly, participants were asked to focus on a spot on the wall at eye level in front of them. Then, they had to cross their arms over the chest and close their eyes. Afterwards, subjects had to undergo the test barefoot standing on one leg on a stable surface, while maintaining balance for as long as possible up to a 45 second period. A stopwatch was used to determine the elapsed time the student was able to maintain unipedal stance up to a maximum of 45 seconds. The trial was disregarded and repeated when participants (1) touched the floor or moved the free foot from the standing limb, (2) uncrossed their arms, (3) moved the standing foot to maintain his balance or (4) opened eyes. Finally, subjects then completed 3 test trials, sitting in a chair to rest for 5 minutes. The average score of the amount of time of three trials was recorded.

  2. Dynamic postural control testing: Star Excursion Balance Test. [1 day]

    Consists of 8 directions, whilst several studies have confirmed the utility of a reduced version of the test using the anterior (ANT), posteromedial (PM) and posterolateral (PL) reaching directions. Participants were required to reach with the free limb for maximal distance in each of three directions and then lightly touch one line, while maintaining his/her balance and without using the free limb for support. Then, 3 trials in each direction for each limb were performed. Visual cues (objects on the floor, people not participating in the study, etc.) were avoided, in order to reduce visual and auditory influences. The trial was repeated when (1) the reach limb touched heavily at the floor, in order to maintain balance or to get any support, (2) moved the stance foot from the grid, (3) failed to return the reach foot to the starting position, or (4) subject's hands did not remain on his/her hips.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 40 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Patients were included if they were healthy university students and were able and willing to complete the protocol
Exclusion Criteria:
  • Had a known musculoskeletal lower extremity injury (eg, postoperative conditions, musculotendinous or ligamentous problems).

  • Previous history of neurological problems.

  • Balance disorders (eg, vestibular or visual problems).

  • Did some type of physical activity programme where balance exercises were performed.

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • University of Valencia

Investigators

  • Principal Investigator: Gemma V Espí-López, PhD, Faculty of Physiotherapy

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
GEMMA V ESPÍ LÓPEZ, PhD, PhD, University of Valencia
ClinicalTrials.gov Identifier:
NCT02508766
Other Study ID Numbers:
  • ID010
First Posted:
Jul 27, 2015
Last Update Posted:
Aug 2, 2016
Last Verified:
Aug 1, 2016
Keywords provided by GEMMA V ESPÍ LÓPEZ, PhD, PhD, University of Valencia

Study Results

No Results Posted as of Aug 2, 2016