DeStress for Health: Partnering With Granville and Vance Counties to Reduce Stress and Cancer Risk (Part 2)
NCT ID: NCT05469334
Last Updated: 2023-05-06
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
14 participants
INTERVENTIONAL
2022-07-14
2022-08-19
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
PREVENTION
NONE
Study Groups
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Experimental: DeStress for Health Program Participants
Rural residents 18 years and older of Granville and Vance counties (n=40) will be recruited to participate.
DeStress for Health Program Participants
Behavioral: DeStress for Health Program The program will consist of 4 in person sessions that are based on empirically supported Positive Psychosocial Well-Being PPWB components including Optimism, Mindfulness, Positive Reprisal as well as Strengths-based Cognitive Behavioral Therapy (SBCBT) to improve behavioral self-regulation towards health-related goals, with an additional class five as a check in that will be used for survey completion. Research staff will conduct face-to-face surveys with participants at baseline and at end of program. Finally, we will conduct a phone-based survey 30 days after program completion to assess sustainability of intervention effects.
Interventions
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DeStress for Health Program Participants
Behavioral: DeStress for Health Program The program will consist of 4 in person sessions that are based on empirically supported Positive Psychosocial Well-Being PPWB components including Optimism, Mindfulness, Positive Reprisal as well as Strengths-based Cognitive Behavioral Therapy (SBCBT) to improve behavioral self-regulation towards health-related goals, with an additional class five as a check in that will be used for survey completion. Research staff will conduct face-to-face surveys with participants at baseline and at end of program. Finally, we will conduct a phone-based survey 30 days after program completion to assess sustainability of intervention effects.
Eligibility Criteria
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Inclusion Criteria
* \>18 years old;
* Interested in participating a stress reduction study
* Speak English
Exclusion Criteria
* Under 18 years of age
* Not interested in participating in a stress reduction study
* does not speak English
18 Years
ALL
Yes
Sponsors
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Duke University
OTHER
Responsible Party
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Principal Investigators
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Devon Noonan, Ph.D
Role: PRINCIPAL_INVESTIGATOR
Duke School of Nursing
Locations
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Granville Vance Public Health Department
Oxford, North Carolina, United States
Countries
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Other Identifiers
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Pro00100183_1
Identifier Type: -
Identifier Source: org_study_id
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