Effects of Ritalin on Postural Stability of Old Adults

Sponsor
Soroka University Medical Center (Other)
Overall Status
Completed
CT.gov ID
NCT00817960
Collaborator
(none)
30
1
1
11
2.7

Study Details

Study Description

Brief Summary

Experimental design overview The proposed project is a prospective experimental study design. independent old adults(age 65 years old and older) who do not suffer from balance problems willing to participate in the study will be tested with well-established measuring techniques of Balance control before and 2 hours after taking of Methylphenidate (Ritalin) in the movement and Rehabilitation Laboratory at BGU. An automated algorithm will be used to extract standardized stabilogram-diffusion parameters from each of the COP data sets collected during quiet standing. These parameters include diffusion coefficients, critical displacement, critical time and scaling exponents for both lateral and anterior-posterior sway directions (Collins & De Luca, 1993). For each of the conditions (before and 1 hour after the use of Ritalin) in three task conditions single task; dual task (concentrating and identifying specific music); and just Listening to a relaxing music. Participants will be required to stand on the platform 10 times for 30 s. For each trial, they will be instructed to sway as little as possible.

Condition or Disease Intervention/Treatment Phase
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
30 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Effects of Methylphenidate on Postural Stability of Old Adults Under Single and Dual Task Conditions.
Study Start Date :
Jul 1, 2011
Actual Primary Completion Date :
Jan 1, 2012
Actual Study Completion Date :
Jun 1, 2012

Arms and Interventions

Arm Intervention/Treatment
Experimental: Methylphenidate

Drug: Methylphenidate
The effect of ritalin on postural stability of old adults (65 years old and over) will be measured using RCT study design

Outcome Measures

Primary Outcome Measures

  1. Postural sway measures [Time 1: pre test' and hour later time 2: post testinng proceedure]

Eligibility Criteria

Criteria

Ages Eligible for Study:
65 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Age 65 years old and older

  • independent elderly adults

  • do not suffer from balance prblems

  • minimental score 24 and above

Exclusion Criteria:
  • old adults who suffer from neurological disease or stroke

  • old adults who suffer from psychiatric state

  • old adults who suffer from orthopedic condition (1/2 a year after a fracture in the lower limb)

  • old adults who suffer from heart conditions

  • old adults who suffer from blindness

Contacts and Locations

Locations

Site City State Country Postal Code
1 SorokaUMC Beer-Sheva Israel 84105

Sponsors and Collaborators

  • Soroka University Medical Center

Investigators

  • Principal Investigator: Itshak Melzer, PhD, Ben-gurion University of the Negev, Beer-Sheva, Israel
  • Study Chair: Zmir Shorer, m, Soroka University Medical Centar
  • Study Director: Yan Press, MD, Soroka University Medical Center

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Soroka University Medical Center
ClinicalTrials.gov Identifier:
NCT00817960
Other Study ID Numbers:
  • SOR476508CTIL
  • MZ4765
First Posted:
Jan 7, 2009
Last Update Posted:
Jun 20, 2012
Last Verified:
Dec 1, 2008
Keywords provided by Soroka University Medical Center
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 20, 2012