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N/A N=22 Other

Compassion Meditation for Older Adults

Anxiety and Mood Disorders

Enrolled (actual)
22
Serious AEs
0.0%
Results posted
Jul 2024
Primary outcome: Primary: Enrollment Rate — 25; 0 Participants

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Compassion Meditation (CM) intervention (Behavioral); Healthy Aging Psychoeducation (Other)
Age
Adult, Older Adult · 55+ yrs
Sex
All
Sponsor
VA Office of Research and Development
Primary completion
Apr 2022

Outcome Measures

OutcomeResultp-value
PRIMARY
Enrollment Rate
25; 0
PRIMARY
Initiation Rate
22
PRIMARY
Completion Rate
13
PRIMARY
Practice Time at Home
SECONDARY
Change in Social Connection (SCS-R) From Baseline to Post-intervention
74.1; 74.8
SECONDARY
Mean (and SD) Change Scores for Each Inflammatory Biomarker (Hs-CRP, IL-6, and TNF- )
SECONDARY
Change in Depression and Anxiety From Baseline to Post-intervention
17.9; 14.9
SECONDARY
Satisfaction With Life (SWLS) From Baseline to Post-intervention
18.0; 21.0
SECONDARY
Change in Positive Emotions (mDES) From Baseline to Post-intervention
21.7; 21.0

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.

Eligibility Criteria

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
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT03964246). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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