MedPath

Compassion Meditation for Older Adults

Not Applicable
Completed
Conditions
Anxiety and Mood Disorders
Interventions
Other: Healthy Aging Psychoeducation
Behavioral: Compassion Meditation (CM) intervention
Registration Number
NCT03964246
Lead Sponsor
VA Office of Research and Development
Brief Summary

Some older Veterans with psychological distress may under-utilize mental health services due to perceived stigma of symptom-focused interventions. This study was designed to examine the feasibility of a strengths-based compassion training intervention with Veterans ages \> 55 years with anxiety or depressive symptoms. Although this study was focused on feasibility if successful, this line of research could open the door to a novel and effective treatment that widens acceptance by older Veterans with psychological distress.

Detailed Description

Many older Veterans in VA primary care clinics experience anxiety and depressive symptoms, but only a minority of these Veterans seek care through VA mental health services. Research suggests that some older Veterans with psychological distress under-utilize mental health services due to perceived stigma of treatments focused on mental health symptoms. However, prior research with civilians, including one study of Veterans with PTSD, suggests a strengths-focused intervention that provides group training in compassion meditation may be effective in reducing negative emotions and increasing positive emotions and well-being. This project was designed to examine the feasibility of this approach with Veterans ages \> 55 years with anxiety or depression. The study was designed to guide and support development of a future larger-size, more definitive follow-up project. . If successful, this line of research could open the door to a novel and effective treatment that widens acceptance by older Veterans with psychological distress.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
25
Inclusion Criteria
  • VA San Diego Healthcare System (VASDHS) patient
  • current mild-to-moderate anxiety or depressive symptoms as defined by scores between 5 and 14 on the Patient Health Questionnaire (PHQ-9) and or Generalized Anxiety Disorders scale (GAD-7).
  • stated intention to attend the 10 group sessions at the scheduled times at the VASDHS in addition to the baseline and follow-up study assessment visits, as well as to complete the outside homework assignments
  • provides written informed consent for participation
Exclusion Criteria
  • no active suicidality/homicidality in the preceding six months
  • untreated alcohol or substance use disorders
  • changes to psychiatric medications within six months prior to the baseline evaluation
  • medical and/or psychiatric instability interfering with current ability to engage in the group sessions and outside homework assignments

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Psychoeducational healthy aging groupHealthy Aging Psychoeducation10-week group focused on review and discussion of psychoeducational videos related to healthy aging topics
Compassion Meditation (CM) intervention groupCompassion Meditation (CM) intervention10-week group intervention consisting of compassion meditation training.
Primary Outcome Measures
NameTimeMethod
Completion Rate12 weeks

The proportion of subjects who complete 6 or more sessions (out of a total of 10 sessions) of intervention among those who start the intervention.

Enrollment Rate36 months

The proportion of consented subjects among all screened and eligible patients.

Initiation Rate4 months

The proportion of subjects who initiate the intervention among all consented subjects.

Practice Time at Home12 weeks

Unanticipated COVID-related restrictions necessitated changing certain outcome measures. Data was not collected for this measure

Secondary Outcome Measures
NameTimeMethod
Change in Social Connection (SCS-R) From Baseline to Post-interventionBaseline and 14 weeks

Social Connectedness Scale (SCS-R), 20-items scores, possible range = 20 to 120, higher scores reflect more connectedness

Change in Depression and Anxiety From Baseline to Post-interventionBaseline and 14 weeks

Brief Symptom Inventory-18 (BSI; depression, anxiety, and somatization) Global Severity Index (GSI). Each of the 18 items range from a score of 0-4; total score ranges from 0-72 with higher scores indicating worse function.

Mean (and SD) Change Scores for Each Inflammatory Biomarker (Hs-CRP, IL-6, and TNF- )14 weeks

The investigators will also examine the mean (and SD) change scores for each inflammatory biomarker (hs-CRP, IL-6, and TNF- ), as well as the association of these changes with practice time.

Satisfaction With Life (SWLS) From Baseline to Post-interventionBaseline and 14 weeks

Satisfaction With Life Scale (SWLS); 5-items, range 5 to 35, higher scores represent greater satisfaction

Change in Positive Emotions (mDES) From Baseline to Post-interventionBaseline and 14 weeks

10-item positive emotions subscale of the 20-item modified Differential Emotions Scale (mDES); scores on this subscale have a potential range of 0 to 40 with higher scores reflecting more positive emotions.

Trial Locations

Locations (1)

VA San Diego Healthcare System, San Diego, CA

🇺🇸

San Diego, California, United States

© Copyright 2025. All Rights Reserved by MedPath