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DeStress for Health: Partnering With Granville and Vance Counties to Reduce Stress and Cancer Risk (Part 2)

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05469334
Enrollment
14
Registered
2022-07-21
Start date
2022-07-14
Completion date
2022-08-19
Last updated
2023-05-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stress Reduction

Keywords

Stress Reduction, Rural, North Carolina, Health Behaviors

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)

Interventions

BEHAVIORALDeStress 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.

Sponsors

Duke University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
Percent of Participants Recommending Intervention to Friend2 monthsMeasured on a scale from 1-5 with 1 being Not at All and 5 being Extremely.
Percentage of Participants That Stay in Study for Duration2 monthsMeasured via subject enrollment log
Percentage of Participants That Attend All Intervention Sessions2 monthsMeasured via subject enrollment log
Percent of Participants Rating Intervention as Useful2 monthsMeasured on a scale from 1-5 with 1 being Not Useful at All and 5 being Extremely Useful.
Number of Participants Recruited in a 6-Month Time-frame6 monthsMeasured via subject enrollment log

Secondary

MeasureTime frameDescription
Change in Positive Emotion As Measured by a Survey2 monthsqualitative scale I agree a lot I agree a little I neither agree nor disagree I disagree a little I disagree a lot
Change in Behavioral Self Regulation As Measured by a Survey2 monthsqualitative scale I agree a lot I agree a little I neither agree nor disagree I disagree a little I disagree a lot
Change in Stress Self Regulation As Measured By a Survey2 monthsqualitative scale I agree a lot I agree a little I neither agree nor disagree I disagree a little I disagree a lot

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026