NCT01241851

Brief Summary

To determine whether acute aerobic exercise versus resistance exercise effects cognitive function among older adults.

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 P50-P75 for early_phase_1

Timeline
Completed

Started Jan 2011

Shorter than P25 for early_phase_1

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

November 15, 2010

Completed
1 day until next milestone

First Posted

Study publicly available on registry

November 16, 2010

Completed
2 months until next milestone

Study Start

First participant enrolled

January 1, 2011

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 1, 2011

Completed
5 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2011

Completed
Last Updated

November 16, 2010

Status Verified

November 1, 2010

Enrollment Period

6 months

First QC Date

November 15, 2010

Last Update Submit

November 15, 2010

Conditions

Cognitive Function in Elderly

Outcome Measures

Primary Outcomes (1)

  • Level of executive function

    One month

Study Arms (3)

Aerobic exercise

ACTIVE COMPARATOR
Behavioral: Aerobic exercise

Resistance exercise

ACTIVE COMPARATOR
Behavioral: Resistance exercise

Control

NO INTERVENTION

Interventions

Aerobic exerciseBEHAVIORAL
Aerobic exercise
Resistance exerciseBEHAVIORAL
Resistance exercise

Eligibility Criteria

Age40 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Exercise at least 2 times a week Able to sign informed consent Able to perform ergometric exam Above 40 years old

You may not qualify if:

  • Smoking
  • Suffering psychiatric or neurologic illness
  • No medication for chronic illness that could effect cognitive function
  • Problems with cognitive functioning after head trauma
  • Long-term hospitalization within the past 3 months
  • Inability to use computer because of vision or motor problems
  • Pregnancy

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Zinman College, Wingate Institute

Netanya, Israel

Location

MeSH Terms

Interventions

ExerciseResistance Training

Intervention Hierarchy (Ancestors)

Motor ActivityMovementMusculoskeletal Physiological PhenomenaMusculoskeletal and Neural Physiological PhenomenaExercise TherapyRehabilitationAftercareContinuity of Patient CarePatient CareTherapeuticsPhysical Therapy ModalitiesPhysical Conditioning, Human

Central Study Contacts

Yael Netz, PhD

CONTACT

972-9-8639362neyael@wincol.ac.il

Study Design

Study Type
interventional
Phase
early phase 1
Allocation
NON RANDOMIZED
Purpose
PREVENTION
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER GOV

Study Record Dates

First Submitted

November 15, 2010

First Posted

November 16, 2010

Study Start

January 1, 2011

Primary Completion

July 1, 2011

Study Completion

December 1, 2011

Last Updated

November 16, 2010

Record last verified: 2010-11

Locations

IL(1)