Trial · NCT06130358
Investigating the Effects of a Museum Intervention on the Psychological and Cardiac Health of Older Adults
NCT06130358, Not applicable, Unknown, Louis Bherer
3 sourcestrials-2026-11-12-0.4.0
Cite this record
ConductScience Library. Investigating the Effects of a Museum Intervention on the Psychological and Cardiac Health of Older Adults. Trials, record NCT06130358. Release trials-2026-11-12-0.4.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT06130358
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Investigating the Effects of a Museum Intervention on the Psychological and Cardiac Health of Older Adults
- NCT number
- NCT06130358
- Status
- Unknown
- Phases
- Not applicable
- Enrollment
- 40 participants, estimated
- Lead sponsor
- Louis Bherer
- Conditions
- Atrial Fibrillation Recurrent, Aging
- Interventions
- Experimental: Well-being intervention followed by classic intervention, Experimental: Classic intervention followed by well-being intervention
- First posted
- 2023-11-14
- Last updated
- 2023-11-18
Source ClinicalTrials.gov
Registered outcomes16
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Change in the activity evoked within the ventrolateral prefrontal cortex during the contemplation of artwork | Before and after the 6 weeks of interventions | Hemodynamic variations in the region of interest (concentration of oxygenated hemoglobin \[HbO2\], no units). |
| Secondary | Change in the activity evoked within the medial prefrontal cortex during the contemplation of artwork | Before and after the 6 weeks of interventions | Hemodynamic variations in the region of interest (concentration of oxygenated hemoglobin \[HbO2\], no units). |
| Other | Change in Heart rate | Before and after the 6 weeks of interventions | bpm |
| Other | Change in arterial pressure | Before and after the 6 weeks of interventions | mmHg |
| Other | Change in salivary cortisol concentration | Before and after the 6 weeks of interventions | microg/l |
| Other | Change in emotionnal regulation | Before and after the 6 weeks of interventions | Difficulties in Emotion Regulation Scale DERS-F scale (Score ranges from 36-180, with a higher score indicating more emotion regulation problems) |
| Other | Change in perceived stress | Before and after the 6 weeks of interventions | Perceived Stress Scale questionnaire (Score ranges from 0-4, with 0 no stress,1 mild stress, 3 moderate stress and 4 severe). |
| Other | Change in Depressive symptomatology | Before and after the 6 weeks of interventions | Geriatric Depression Scale questionnaire (Score ranges from 0-30, with a higher score indicating larger depressive symptomatology). |
| Other | Change in Quality-of-life | Before and after the 6 weeks of interventions | 36-Item Short Form Health Survey (Scale ranges from 0-100, with a higher score indicating a better health status). |
| Other | Change in Perceived social support | Before and after the 6 weeks of interventions | Lubben Social Network Scale questionnaire (Score ranges from 0-30, with a higher score indicating more social engagement). |
1 to 10 of 16Source ClinicalTrials.gov
See all 16 registered outcomesOutcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
Grants0
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.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests1
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 |
|---|---|
| Stroop Color-Word Test | Other outcome |
Source ConductCognition
Source
- Release
- trials-2026-11-12-0.4.0
- Release manifest SHA-256
- 0f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4
- Registry capture
- 2026-11-12
- Results copy, AACT
- 2026-03-23
- NIH clinical studies file
- 2026-11-13
Source ClinicalTrials.gov
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNone stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.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.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT06130358
GET https://conductscience.org/api/trials/v1/NCT06130358/registered