Improving Mental Health and Well-Being Via Awe Walks
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| ClinicalTrials.gov Identifier: NCT03550144 |
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Recruitment Status :
Completed
First Posted : June 8, 2018
Last Update Posted : October 12, 2018
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| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| Awe Compassion Anxiety | Behavioral: Awe Walk Behavioral: Control Walk | Not Applicable |
| Study Type : | Interventional (Clinical Trial) |
| Actual Enrollment : | 60 participants |
| Allocation: | Randomized |
| Intervention Model: | Parallel Assignment |
| Masking: | Single (Participant) |
| Primary Purpose: | Prevention |
| Official Title: | Effects of Awe on Mental Health and Well-Being |
| Actual Study Start Date : | December 5, 2016 |
| Actual Primary Completion Date : | December 10, 2017 |
| Actual Study Completion Date : | May 26, 2018 |
| Arm | Intervention/treatment |
|---|---|
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Experimental: Awe Walk Condition
Participants were instructed to take at least one (~15 minute) walk per week for 8 consecutive weeks. Participants were told to seek the experience of feeling awe. Participants were told to keep a fairly light to moderate pace and were encouraged to walk alone and without interruption from a mobile device.
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Behavioral: Awe Walk
To examine the effect of weekly awe walks in cognitively healthy older adults. |
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Active Comparator: Control Walk Condition
Participants were instructed to take at least one (~15 minute) walk per week for 8 consecutive weeks. Participants were told to keep a fairly light to moderate pace and were encouraged to walk alone and without interruption from a mobile device.
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Behavioral: Control Walk
To examine the effect of weekly walks in cognitively healthy older adults. |
- Daily awe experience questionnaire [ Time Frame: 8 weeks ]Increase in awe experience
- Daily compassion experience questionnaire [ Time Frame: 8 weeks ]Increase in daily compassion experience
- Daily negative emotional experience questionnaire [ Time Frame: 8 weeks ]Decrease in daily negative emotional experience
- Generalized Anxiety Disorder- 7 Item Scale [ Time Frame: 8 weeks ]Decrease in anxiety
- Satisfaction With Life Scale [ Time Frame: 8 weeks ]Increase in well-being
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| Ages Eligible for Study: | 40 Years to 90 Years (Adult, Older Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
- Stable medical condition for 3 months prior to screening
- Reliant informant with frequent contact with participant who is available to provide observations of participant
- Fluent in English or Spanish
- Age: 40 and above
- Able to complete baseline assessments
- Education or work history sufficient to exclude mental retardation
- Physically acceptable for this study as confirmed by medical history, physical exam, neurological exam and clinical tests
Exclusion Criteria:
- Major memory concerns/diagnosed memory condition
- Korsakoff encephalopathy
- Active substance abuse
- Brain tumor
- Active neoplastic disease (skin tumors other than melanoma are not exclusionary)
- Parkinson's disease
- Multiple sclerosis (untreated)
- Sleep apnea
- History of clinically significant stroke
- Current evidence or history in the past 2 years of epilepsy, focal brain lesion, cancer, steroid use, or DSM-IV criteria for any major psychiatric disorder including psychosis, major depression, bipolar disorder, alcohol or substance abuse
- Blindness, deafness, language difficulties or any other disability which may prevent the participant from participating or cooperating in the protocol
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03550144
| United States, California | |
| UCSF Memory and Aging Center | |
| San Francisco, California, United States, 94158 | |
| Principal Investigator: | Virginia E Sturm, PhD | University of California, San Francisco |
Documents provided by Virginia Sturm, PhD, University of California, San Francisco:
Publications:
| Responsible Party: | Virginia Sturm, PhD, Assistant Professor, University of California, San Francisco |
| ClinicalTrials.gov Identifier: | NCT03550144 |
| Other Study ID Numbers: |
16-20001 |
| First Posted: | June 8, 2018 Key Record Dates |
| Last Update Posted: | October 12, 2018 |
| Last Verified: | May 2018 |
| Individual Participant Data (IPD) Sharing Statement: | |
| Plan to Share IPD: | Undecided |
| Studies a U.S. FDA-regulated Drug Product: | No |
| Studies a U.S. FDA-regulated Device Product: | No |
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Awe Compassion Anxiety Positive emotions Aging |

