Stress Management Training for Healthy Aging
NCT02888600, Not applicable, Completed, Carnegie Mellon University
Trial 10
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
| Field | Value | Source |
|---|---|---|
| Title | Stress Management Training for Healthy Aging | ClinicalTrials.gov |
| NCT number | NCT02888600 | ClinicalTrials.gov |
| Status | Completed | ClinicalTrials.gov |
| Phases | Not applicable | ClinicalTrials.gov |
| Enrollment | 190 participants, actual | ClinicalTrials.gov |
| Lead sponsor | Carnegie Mellon University | ClinicalTrials.gov |
| Conditions | Psychological Stress, Loneliness | ClinicalTrials.gov |
| Interventions | Mindfulness Training, Health Education | ClinicalTrials.gov |
| First posted | 2016-09-05 | ClinicalTrials.gov |
| Last updated | 2024-10-23 | ClinicalTrials.gov |
Registered outcomes 34
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description | Source |
|---|---|---|---|---|
| Primary | Circulating markers of inflammation, Interleukin-6 and C Reactive Protein | Change from baseline to 1-week post-intervention and 3-month follow-up | Measured via blood samples | ClinicalTrials.gov |
| Secondary | Pro-inflammatory gene expression | Change from baseline to 1-week post-intervention | ClinicalTrials.gov | |
| Secondary | Self-reported relational distress | Change from Baseline to Intervention Weeks 4 and 8 | Evaluated using ecological momentary assessment | ClinicalTrials.gov |
| Secondary | Self-reported loneliness | Change from baseline to 1-week post-intervention and 3-month follow-up | Evaluated using UCLA loneliness scale and ecological momentary assessment | ClinicalTrials.gov |
| Secondary | Self-reported awareness of experiences and reactivity to experience during resting state | 1-week post-intervention and 3-month follow-up | Questionnaire assessing the frequency in which participants notice a variety of positive, neutral, and negative experiences and their reactivity to those experiences during a 5-minute resting state period | ClinicalTrials.gov |
| Secondary | Working memory in daily living | Change from baseline to intervention weeks 4 and 8 | Assessed via a dot memory ambulatory smartphone-based task administered at six timepoints per day, for three days in a row, at baseline and at Intervention weeks 4 and 8 | ClinicalTrials.gov |
| Secondary | Implicit acceptance of self | 1-week post-intervention and 3-month follow-up | Assessed via an Implicit Association Test (IAT) behaviorally quantifying the association between self and acceptance/judgment | ClinicalTrials.gov |
| Other | Health practices | Change from baseline to 1-week post-intervention and 3-month follow-up | Evaluated by questionnaires asking about diet, caffeine consumption, alcohol use, stress reduction, exercise, recreational drug use, cold or flu, flu shots | ClinicalTrials.gov |
| Other | Mental health | Change from baseline to 1-week post-intervention and 3-month follow-up | Evaluated using Beck Depression Inventory | ClinicalTrials.gov |
| Other | Self-reported stress | Change from baseline to 1-week post-intervention and 3-month follow-up | ClinicalTrials.gov | |
| Other | Mindfulness | Change from baseline to 1-week post-intervention and 3-month follow-up | Evaluated using Mindful Attention Awareness Scale | ClinicalTrials.gov |
| Other | Connectedness to nature | Change from baseline to 1-week post-intervention and 3-month follow-up | Evaluated using Nature Connection Scale | ClinicalTrials.gov |
| Other | Personality | Change from baseline to 1-week post-intervention and 3-month follow-up | Evaluated using NEO Personality Inventory | ClinicalTrials.gov |
| Other | Social network and social support | Change from baseline to 1-week post-intervention and 3-month follow-up | Evaluated using Social Network Index and Interpersonal Support Evaluation List | ClinicalTrials.gov |
| Other | Self-reported psychological distress | Change from baseline to 1-week post-intervention and 3-month follow-up | ClinicalTrials.gov | |
| Other | Trait affect | Change from baseline to 1-week post-intervention and 3-month follow-up | Evaluated using Stanford Measure of Actual, Ideal, and Avoided Affect | ClinicalTrials.gov |
| Other | Trait hostility | Change from baseline to 1-week post-intervention and 3-month follow-up | Evaluated using Cook-Medley Hostility Scale | ClinicalTrials.gov |
| Other | Attachment style | Change from baseline to 1-week post-intervention and 3-month follow-up | Evaluated using Adult Attachment Scale | ClinicalTrials.gov |
| Other | Attitudes towards aging | Change from baseline to 1-week post-intervention and 3-month follow-up | Evaluated using Attitudes to Aging Questionnaire | ClinicalTrials.gov |
| Other | Immune functioning | Change from baseline to 1-week post-intervention and 3-month follow-up | Assessed via stimulated IL-6 production and glucocorticoid resistance | ClinicalTrials.gov |
Outcomes 0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
| Type | Outcome | Time frame | Population | Units | Measured as | Source |
|---|
Results by group 0
Each measurement the trial posted, group by group, in the words and numbers it posted.
| Outcome | Group | Category | Value | Spread | Units | Source |
|---|
Participant flow 0
How many started, completed or left each group, period by period.
| Period | Milestone | Group | Participants | Units counted | Source |
|---|
Adverse events 0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
| Type | Event | Organ system | Group | Affected | At risk | Events | Source |
|---|
Adverse event totals 0
The totals the trial posted for each group.
| Total | Group | Affected | At risk | Source |
|---|
Papers 2
The papers the trial lists on ClinicalTrials.gov.
Grants 1
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
| Project | Title | Principal investigators | Organization | Funder | Fiscal years | Source |
|---|---|---|---|---|---|---|
| R01AT008685 | Mindfulness Meditation Training in Lonely Older Adults | CRESWELL, JOHN DAVID | CARNEGIE-MELLON UNIVERSITY | NATIONAL CENTER FOR COMPLEMENTARY & INTEGRATIVE HEALTH | 2015 to 2019 | NIH RePORTER |
Trial comparisons 0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
| Comparison | Source |
|---|
Tests 5
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
| Test | Named as | Source |
|---|---|---|
| Dichotic Listening Task | Other outcome | ConductCognition |
| Emotional Stroop Task | Other outcome | ConductCognition |
| Implicit Association Test (IAT) | Secondary outcome | ConductCognition |
| Stroop Color-Word Test | Other outcome | ConductCognition |
| Symbol Scan Task | Other outcome | ConductCognition |
Source 5
| Field | Value | Source |
|---|---|---|
| Release | trials-2026-11-12-0.4.0 | ClinicalTrials.gov |
| Release manifest SHA-256 | 0f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4 | ClinicalTrials.gov |
| Registry capture | 2026-11-12 | ClinicalTrials.gov |
| Results copy, AACT | 2026-03-23 | ClinicalTrials.gov |
| NIH clinical studies file | 2026-11-13 | ClinicalTrials.gov |
Release trials-2026-11-12-0.4.0
ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299 ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
ClinicalTrials.gov: none stated ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
NIH RePORTER's clinical studies and project files: Public domain (NIH RePORTER)