CClinicalTrials.gg
CompletedNCT01909921Updated May 17, 2016

Retrospective Medical Record Review of Mind Body Depression Group Participants

An observational study in Depression and Anxiety, sponsored by Massachusetts General Hospital. Completed. Open to participants aged 21 Years and older. Per ClinicalTrials.gov, last updated 2016-05-17.

Sponsored by Massachusetts General Hospital · Observational

Study type
Observational
Model
Case-only
Time perspective
Retrospective
Enrollment
156
Ages
21 Years and older
Sex
All
01

Study 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.

Read the detailed description

This is a retrospective review of medical records. The study aims to evaluate the effects of participation in the Relaxation Response Intervention for Depression Clinical groups, on patient measures of: 1) depression, anxiety and perceived stress; 2) work productivity and activity impairment; 3) demand for, and adherence to behavioral medicine; 4) medication use for depression and/or anxiety; and 5) dose-response effects.

02

Conditions studied

  • Depression
  • Anxiety
03

In context

Depression

8,057 studies on the registry are indexed under Depression; 1,641 are open to participants now.

This study's enrollment of 156 is close to the median of 160 across 1,084 observational studies indexed under Depression.

Browse Depression studies →

Lead sponsor

Massachusetts General Hospital is the lead sponsor of 2,536 studies on the registry; 446 are open to participants now.

Of its 214 completed or terminated interventional studies of FDA-regulated products, 161 (75%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
21 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

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

Inclusion criteria

  • Patients receiving care through MGH-Health Centers
  • a diagnosis of depression and/or anxiety
  • 21 years of age or older

Exclusion criteria

Exclusion Criteria:

-

05

Study design

Observational model
Case-only
Time perspective
Retrospective
Enrollment
156 participants (actual)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. Change from baseline in Depression scales (CES-D 10) at 8 weeks

    Time frame: Pre- and Post-Intervention (8 weeks)

  2. Change from baseline Anxiety Scales (STAI-20) at 8 weeks

    Time frame: Pre- and Post- Intervention (8 weeks)

  3. Change from baseline in Perceived Stress Scale (PSS-10) at 8 weeks

    Time frame: Pre- and Post-Intervention (8 weeks)

07

Study locations

No study locations are listed for this record.

08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 17, 2016, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01909921
Lead sponsor
Massachusetts General Hospital
Responsible party
John W. Denninger, MD, PhD (Director of Research at the Benson-Henry Institute for Mind Body Medicine, Massachusetts General Hospital) — Principal investigator
First posted
Jul 29, 2013
Start date
Jan 2009
Primary completion
Dec 2012
Completion
Mar 2015
Last update
May 17, 2016

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in May 2016. You cannot join it, but the record below documents what was studied.

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