NCT01909921

Completed

Retrospective Medical Record Review of Mind Body Depression ...

Massachusetts General Hospital Source

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Other study identifiers

Sponsor study identifier

2010P001513

Study Type

observational

Actual enrollment (reported)

156

Locations

0 countries

Sites

N/A

Timeline

Study Start

January 2009

Date type not reported

This date has not been verified as actual or estimated.

Primary Completion

December 2012

Actual (reported)

Study Completion

March 2015

Actual (reported)

Brief Summary

The purpose of this study is to assess the effectiveness of a Relaxation Response Intervention for Depression offered to low income populations at Massachusetts General Hospital (MGH) - Chelsea, Revere and Charlestown health centers.

Registry Overview

Registry-reported information. Elapsed time and enrollment totals alone do not measure study progress or recruitment pace.

Recruitment status: completed
Actual enrollment (reported): 156 participants
Study completion date: March 2015
Actual (reported)
Listed locations: 0 countries · 0 sites

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Dates and qualifiers reported by the registry. Estimated dates do not confirm that a milestone has occurred.

Study Start
January 2009
Date type not reported
This date has not been verified as actual or estimated.
Primary Completion
December 2012
Actual (reported)
First Submitted
May 28, 2013
Actual (reported)
First Posted
July 29, 2013
Actual (reported)
Study Completion
March 2015
Actual (reported)

Last Updated: May 17, 2016
Status Verified: May 2016
Last Update Submitted: May 16, 2016

Conditions

Anxiety Depression

Outcome Measures

Primary Outcomes (3)

Change from baseline in Depression scales (CES-D 10) at 8 weeks
Pre- and Post-Intervention (8 weeks)
Change from baseline Anxiety Scales (STAI-20) at 8 weeks
Pre- and Post- Intervention (8 weeks)
Change from baseline in Perceived Stress Scale (PSS-10) at 8 weeks
Pre- and Post-Intervention (8 weeks)

Eligibility Criteria

Age21 Years+

Sexall

Healthy VolunteersNo

Age GroupsAdult (18-64), Older Adult (65+)

Sampling MethodNon-Probability Sample

Study Population

MGH-Health Center patients who have participated in the Relaxation Response Intervention for Depression groups.

You may qualify if:

Patients receiving care through MGH-Health Centers

Sponsors & Collaborators

Massachusetts General Hospital
Otherlead

MeSH Terms

Conditions

DepressionAnxiety Disorders

Condition Hierarchy (Ancestors)

Behavioral SymptomsBehaviorMental Disorders

Enrollment

156 participants (actual enrollment reported by the registry).

Study Design

Study Type: observational
Observational Model: CASE ONLY
Time Perspective: RETROSPECTIVE
Sponsor Type: OTHER
Responsible Party: PRINCIPAL INVESTIGATOR
PI Title: Director of Research at the Benson-Henry Institute for Mind Body Medicine

Study Record Dates

First Submitted

May 28, 2013

First Posted

July 29, 2013

Study Start

January 2009

Date type not reported

This date has not been verified as actual or estimated.

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NCT00663078

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a diagnosis of depression and/or anxiety

years of age or older

Contact the study team to confirm eligibility.

Primary Completion

December 2012

Actual (reported)

Study Completion

March 2015

Actual (reported)

Last Updated

May 17, 2016

Record last verified: 2016-05

Source record

Download the complete ClinicalTrials.gov record imported by Syfrah, including fields not shown in this page. The registry may contain a newer revision.

Source: ClinicalTrials.gov.

JSON downloads include source attribution and retrieval details alongside the unchanged original record or the separately normalized values.

Registry identifier: NCT01909921
Data provider: ClinicalTrials.gov
Source updated: 2016-05-17
Normalization version: ctgov-legacy-1

Open registry record

Source retrieved: 2026-10-25 22:21:32 UTC

Brief Summary

Registry Overview

Trial Relationships

Related Scientific Literature

Study Timeline

Study Start

Primary Completion

First Submitted

First Posted

Study Completion

Conditions

Outcome Measures

Primary Outcomes (3)

Eligibility Criteria

You may qualify if:

Sponsors & Collaborators

MeSH Terms

Conditions

Condition Hierarchy (Ancestors)

Enrollment

Study Design

Study Record Dates

Source record