The Effect of Relaxation Response Training on Declarative... | NCT00179530

Studies
The Effect of Relaxation Response Training on Declarative Memory and Salivary Cortisol in Older Adults

NCT00179530

Sponsor

Beth Israel Deaconess Medical Center

Status

Completed

Last Update Posted

Nov 5, 2007Estimated

Enrollment

16Actual

Phase

Phase 2

Conditions

Healthy

Interventions

Relaxation Response

Countries

Not provided

Protocol Section

Identification Module Status Module Sponsor/Collaborators Module Oversight Module Description Module Conditions Module Design Module Arms/Interventions Module Outcomes Module Eligibility Module Contacts/Locations Module References Module IPD Sharing Statement Module

Results Section

Participant Flow Module Baseline Characteristics Module Outcome Measures Module Adverse Events Module More Info Module

Annotation Section

Annotation Module

Document Section

Large Document Module

Derived Section

Miscellaneous Info Module Condition Browse Module Intervention Browse Module

Protocol Section

Identification Module

NCT ID

Results Section

No data available

No data is available for this block.

Annotation Section

No data available

No data is available for this block.

Document Section

No data available

No data is available for this block.

Derived Section

Miscellaneous Info Module

Version Holder

Status Module

Record Verification Date

Nov 2007

Overall Recruitment Status or Expanded Access Status

Completed

Last Known Status

Not provided

Delayed Posting

Not provided

Why Stopped

Not provided

Expanded Access Info

Start Date

May 1999

Primary Completion Date

Not provided

Completion Date

Sep 2007Actual

First Submitted Date

Sep 13, 2005

First Submission Date that Met QC Criteria

Sep 13, 2005

First Posted Date

Sep 16, 2005Estimated

Results Waived

Not provided

Results First Submitted Date

Not provided

Results First Submitted that Met QC Criteria

Not provided

Results First Posted Date

Not provided

Certification/Extension (aka Delayed Results) First Submitted Date

Not provided

Certification/Extension First Submitted that Passed QC Review

Not provided

Certification/Extension First Posted Date

Not provided

Last Update Submitted Date

Nov 2, 2007

Last Update Posted Date

Nov 5, 2007Estimated

Description Module

Brief Summary

To evaluate whether a 5-week relaxation response intervention influences the learning, memory or attention of healthy older adults.

Detailed Description

Not provided

Design Module

Study Type

Interventional

Number of References to an Expanded Access Study

Not provided

Expanded Access Types

Not provided

Patient Registry

Not provided

Target Follow-Up Duration

Not provided

Phases

Phase 2

Interventional Study Design

Allocation

Biospecimen

No data available

No data is available for this block.

Enrollment

16Actual

Name	Type	Description	Arm Group Labels	Other Names
Relaxation Response	Behavioral	Relaxation training

Outcomes Module

Primary Outcomes

Measure	Description	Time Frame
Evaluate whether a RR training program would decrease anxiety levels, improve attention, declarative memory performance in healthy older adults.		8 weeks

Secondary Outcomes

Measure	Description	Time Frame
Evaluate whether a RR training program would decrease salivary cortisol levels in healthy older adults.		8 weeks

Other Outcomes

Not provided

Eligibility Module

Eligibility Criteria

Inclusion Criteria:

65 to 80 years od age
No prior or current psychiatric or neurological condition.
score above 24 on the Mini-Mental State Exam (MMSE)

Accepts Healthy Volunteers

Yes

Sex

All

Sex/Gender Based

Not provided

Sex/Gender Description

Not provided

Minimum Age

65 Years

Maximum Age

80 Years

Standard Ages

Older Adult

Study Population

Not provided

Sampling Method

Not provided

Contacts/Locations Module

Central Contacts

Not provided

Overall Officials

Name	Affiliation	Role
Jeffery A Dusek, PhD	Beth Israel Deaconess Medical Center, Mind/Body Medical Institute	Principal Investigator

Locations

Not provided