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Effect of Core Stability Exercise Versus Whole Body Vibration in Improving Vitamin D Absorption in Women

NCT06721637 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 40

Last updated 2024-12-11

No results posted yet for this study

Summary

This study was conducted to explore the influence of core stability exercise versus whole body vibration in improving vitamin D absorption in women.

Conditions

  • Vitamin D Absorption

Interventions

COMBINATION_PRODUCT

Group A (n = 20): received core stability exercise trained three times a week for 8 weeks.

Woman was in crook lying position with feet flat on the treatment table. The therapist put his two thumbs on the anterior superior iliac spines then, asked the woman to contract the abdominal muscle, hold the contraction for 10 seconds, then, asked her to relax for 10 seconds

DEVICE

Group B (n = 20): received whole body vibration trained three times a week for 8 weeks

The woman assumed a full squat position on a vibration platform. The apparatus was set at a frequency of 30 Hz, amplitude of 2 mm, and duration of 5 min. The women were instructed to remain in the squatting position with holding hand rail after turning on the vibration and to report any discomfort that might arise. At the end of 5 min, the vibration turned off automatically. Thereafter, the women took a 1-min rest. They were then asked to stand on the vibration platform for 5 min, with the same parameters as those used in the squatting position. Thus, the total time for the application of WBV in each session was 10 min

Sponsors & Collaborators

  • October 6 University

    lead OTHER

Eligibility

Min Age
20 Years
Max Age
50 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-06-09
Primary Completion
2024-07-15
Completion
2024-11-25

Countries

  • Egypt

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06721637 on ClinicalTrials.gov