NCT02476344

Brief Summary

2 young candidates have tragically died during army pre-recruitment sorting series in 2006. As part of the classification and characterization of the physical aspects of the training, this experiment was requested. We aim at determining the characteristics of physical strains in sorting series, by objective and subjective parameters and evaluating the difficulty levels and intensity of those strains.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
40

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Jul 2015

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

June 17, 2015

Completed
2 days until next milestone

First Posted

Study publicly available on registry

June 19, 2015

Completed
12 days until next milestone

Study Start

First participant enrolled

July 1, 2015

Completed
1 year until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 1, 2016

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

October 1, 2016

Completed
Last Updated

July 14, 2015

Status Verified

July 1, 2015

Enrollment Period

1 year

First QC Date

June 17, 2015

Last Update Submit

July 12, 2015

Conditions

Outcome Measures

Primary Outcomes (1)

  • heart rate will be monitored using a wearable heart rate monitor (Polar® sensor and heart rate monitor watch)

    The heart rate will be monitored using a wearable heart rate monitor (Polar® sensor and heart rate monitor watch).

    3 experiment days

Secondary Outcomes (3)

  • CPK measured from blood sample (3ml) in the lab

    3 experiment days

  • lactic acid measured using lactat-meter (Lactate pro LT-1710)

    3 experiment days

  • body core temperature monitored using telemetry pill

    3 experiment days

Study Arms (1)

research arm

EXPERIMENTAL

40 subjects will undergo the experiment protocol, total 3 days, each consisting different training exercises.

Other: experiment protocol

Interventions

each subject will perform the following 3 days experiment protocol, consisting of army training exercises: 1. sack carrying exercise. 2. crawling exercise. 3. combined exercise: sack carrying, crawling and sprints. heart rate, core temperature, lactic acid and CPK levels will be monitored continuously.

research arm

Eligibility Criteria

Age18 Years - 22 Years
Sexmale
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Aged 18-22 years.
  • Healthy civilian volunteers.
  • without skeleton-muscle illnesses.
  • without Infectious disease 2 weeks prior to the experiment.

You may not qualify if:

  • any physical condition.
  • physician decition.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Sheba medical center

Tel Litwinsky, Ramat- Gan, Israel

Location

MeSH Terms

Conditions

Motor Activity

Condition Hierarchy (Ancestors)

Behavior

Study Officials

  • Ofir Frenkel, M.D

    Sheba Medical Center

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
PREVENTION
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER GOV
Responsible Party
SPONSOR

Study Record Dates

First Submitted

June 17, 2015

First Posted

June 19, 2015

Study Start

July 1, 2015

Primary Completion

July 1, 2016

Study Completion

October 1, 2016

Last Updated

July 14, 2015

Record last verified: 2015-07

Locations