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Clinical Trials/NCT05469334
NCT05469334
Completed
Not Applicable

DeStress for Health: Partnering With Granville and Vance Counties to Reduce Stress and Cancer Risk

Duke University1 site in 1 country14 target enrollmentJuly 14, 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Stress Reduction
Sponsor
Duke University
Enrollment
14
Locations
1
Primary Endpoint
Number of Participants Recruited in a 6-Month Time-frame
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

The purpose of this research study is to determine whether a positive psychology intervention paired with a health behavior intervention is successful in decreasing perceived stress and increasing positive affect in residents of Vance and Granville County.The program will consist of 4 in person / zoom sessions that are based on empirically supported PPWB components including Optimism, Gratitude, Mindfulness and Positive Savoring 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. Specifically, principal investigator will provide participants with instruction on positive psychology exercises that can do on their own and counseling around increased fruit and vegetable intake, physical activity and smoking cessation. Participants will then be asked to create a SMART goal to work on each week of the program for one of the behaviors. Research staff will conduct surveys with participants at baseline and at end of program. Feasibility and acceptability measures of the intervention will be collected at the end of the program. Research team will also collect informal feedback from participants at the end of each of the class sessions. Classes will be delivered in person and broadcasted via zoom via a password protected zoom link. Participant who choose to remain remote and participate via Zoom will be mailed binders of study materials with information on who to call if participants have questions. Participants who attend live events will receive their materials in person. Pre- and post-intervention surveys will be sent to participants via email. This is Part 2 of study (NCT03776890)

Registry
clinicaltrials.gov
Start Date
July 14, 2022
End Date
August 19, 2022
Last Updated
2 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Live in Granville or Vance Counties;
  • \>18 years old;
  • Interested in participating a stress reduction study
  • Speak English

Exclusion Criteria

  • Does Not Live in Granville or Vance Counties
  • Under 18 years of age
  • Not interested in participating in a stress reduction study
  • does not speak English

Outcomes

Primary Outcomes

Number of Participants Recruited in a 6-Month Time-frame

Time Frame: 6 months

Measured via subject enrollment log

Percentage of Participants That Attend All Intervention Sessions

Time Frame: 2 months

Measured via subject enrollment log

Percentage of Participants That Stay in Study for Duration

Time Frame: 2 months

Measured via subject enrollment log

Percent of Participants Rating Intervention as Useful

Time Frame: 2 months

Measured on a scale from 1-5 with 1 being "Not Useful at All" and 5 being "Extremely Useful".

Percent of Participants Recommending Intervention to Friend

Time Frame: 2 months

Measured on a scale from 1-5 with 1 being "Not at All" and 5 being "Extremely".

Secondary Outcomes

  • Change in Positive Emotion As Measured by a Survey(2 months)
  • Change in Behavioral Self Regulation As Measured by a Survey(2 months)
  • Change in Stress Self Regulation As Measured By a Survey(2 months)

Study Sites (1)

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