Trial Outcomes & Findings for The Heart of the Community Study (NCT NCT05560893)
NCT ID: NCT05560893
Last Updated: 2026-08-10
Results Overview
Cardiovascular health was assessed using heart rate variability (HRV) measured during a socially relevant stressor task administered in each intervention session. HRV data were collected using the movisens device, a wearable chest-mounted sensor that records electrocardiogram (ECG) data. Vagally mediated HRV was calculated from the variability of inter-beat (R-R) intervals derived from these ECG recordings. Mean HRV values were calculated for each assessment period, with higher mean HRV values (per minute) indicating greater autonomic regulation and improved cardiovascular health. Due to feasibility and data quality issues with the wearable ECG device, HRV data collection was discontinued after the first two assessment periods (Baseline 1 and the 4-week assessment \[post-intervention for the intervention group/Baseline 2 for the waitlist control group\]); therefore, post-intervention HRV data were not collected for the waitlist control group.
COMPLETED
NA
84 participants
Assessed at Baseline 1 for both groups and 4 weeks later (post-intervention for intervention participants and Baseline 2 for waitlist control participants). Post-intervention data were not collected for the waitlist control group.
2026-08-10
Participant Flow
Participants in this study (N = 84; 92% female) were recruited from 12 community service agencies that primarily serve low-income Hispanic/Latine (HL) families
No significant events occurred between enrollment and assignment to study groups. Of the 84 participants to begin the RS intervention, 80 completed all four intervention sessions; 78 completed the post-intervention assessment; and 62 completed the 3-month follow-up assessment.
Participant milestones
| Measure |
Intervention Group
After providing informed consent, participants completed a baseline assessment. CSPs assigned to the intervention group (n = 41) then completed the 4-week intervention, followed by a post-intervention assessment administered immediately afterward and a 3-month follow-up assessment.
|
Waitlist Control Group
After providing informed consent, participants assigned to the waitlist control group (n = 43) completed a baseline assessment and did not receive the intervention for the subsequent 4 weeks. At the end of this period, they completed a second baseline assessment (BL2) prior to beginning the intervention. Participants then completed additional assessments immediately post-intervention (8-weeks from enrollment) and again at a 3-month follow-up.
|
|---|---|---|
|
Baseline 1
STARTED
|
41
|
43
|
|
Baseline 1
COMPLETED
|
41
|
43
|
|
Baseline 1
NOT COMPLETED
|
0
|
0
|
|
Baseline 2
STARTED
|
0
|
43
|
|
Baseline 2
COMPLETED
|
0
|
42
|
|
Baseline 2
NOT COMPLETED
|
0
|
1
|
|
Intervention
STARTED
|
41
|
42
|
|
Intervention
COMPLETED
|
40
|
40
|
|
Intervention
NOT COMPLETED
|
1
|
2
|
|
Post-Intervention
STARTED
|
40
|
40
|
|
Post-Intervention
COMPLETED
|
39
|
39
|
|
Post-Intervention
NOT COMPLETED
|
1
|
1
|
|
3-Month Follow Up
STARTED
|
39
|
39
|
|
3-Month Follow Up
COMPLETED
|
31
|
31
|
|
3-Month Follow Up
NOT COMPLETED
|
8
|
8
|
Reasons for withdrawal
| Measure |
Intervention Group
After providing informed consent, participants completed a baseline assessment. CSPs assigned to the intervention group (n = 41) then completed the 4-week intervention, followed by a post-intervention assessment administered immediately afterward and a 3-month follow-up assessment.
|
Waitlist Control Group
After providing informed consent, participants assigned to the waitlist control group (n = 43) completed a baseline assessment and did not receive the intervention for the subsequent 4 weeks. At the end of this period, they completed a second baseline assessment (BL2) prior to beginning the intervention. Participants then completed additional assessments immediately post-intervention (8-weeks from enrollment) and again at a 3-month follow-up.
|
|---|---|---|
|
Baseline 2
Lost to Follow-up
|
0
|
1
|
|
Intervention
Lost to Follow-up
|
1
|
2
|
|
Post-Intervention
Lost to Follow-up
|
1
|
1
|
|
3-Month Follow Up
Lost to Follow-up
|
8
|
8
|
Baseline Characteristics
The Heart of the Community Study
Baseline characteristics by cohort
| Measure |
Intervention Group
n=41 Participants
Following a baseline assessment, CSPs assigned to the intervention group (n = 41) received the intervention immediately. Participants completed an identical assessment battery at pre-intervention baseline, immediately post-intervention, and 3 months following the intervention.
|
Waitlist Control Group
n=43 Participants
Following a baseline assessment, CSPs assigned to the waitlist group (n = 43) did not receive the intervention for 4 weeks and completed a second baseline assessment prior to receiving the intervention. Participants completed the same assessment battery at pre-intervention baseline, immediately post-intervention, and 3 months following the intervention.
|
Total
n=84 Participants
Total of all reporting groups
|
|---|---|---|---|
|
Age, Continuous
|
49.51 years
STANDARD_DEVIATION 10.87 • n=54 Participants
|
47.12 years
STANDARD_DEVIATION 11.30 • n=54 Participants
|
48.10 years
STANDARD_DEVIATION 11.05 • n=27 Participants
|
|
Sex: Female, Male
Female
|
41 Participants
n=54 Participants
|
37 Participants
n=54 Participants
|
78 Participants
n=27 Participants
|
|
Sex: Female, Male
Male
|
0 Participants
n=54 Participants
|
6 Participants
n=54 Participants
|
6 Participants
n=27 Participants
|
|
Race/Ethnicity, Customized
Latine
|
40 Participants
n=54 Participants
|
40 Participants
n=54 Participants
|
80 Participants
n=27 Participants
|
|
Race/Ethnicity, Customized
Black/African American
|
1 Participants
n=54 Participants
|
1 Participants
n=54 Participants
|
2 Participants
n=27 Participants
|
|
Race/Ethnicity, Customized
Other (not specified)
|
0 Participants
n=54 Participants
|
2 Participants
n=54 Participants
|
2 Participants
n=27 Participants
|
|
Number of Children
|
2.78 number of chidren
STANDARD_DEVIATION 1.20 • n=54 Participants
|
2.88 number of chidren
STANDARD_DEVIATION 1.43 • n=54 Participants
|
2.82 number of chidren
STANDARD_DEVIATION 1.31 • n=27 Participants
|
|
US Born
|
7 participants
n=54 Participants
|
8 participants
n=54 Participants
|
15 participants
n=27 Participants
|
|
Education level
|
11.38 years
STANDARD_DEVIATION 2.08 • n=54 Participants
|
11.09 years
STANDARD_DEVIATION 3.16 • n=54 Participants
|
11.25 years
STANDARD_DEVIATION 2.64 • n=27 Participants
|
|
Years as CHW for current agency
|
5.13 years
STANDARD_DEVIATION 5.61 • n=54 Participants
|
4.80 years
STANDARD_DEVIATION 4.89 • n=54 Participants
|
5.04 years
STANDARD_DEVIATION 5.16 • n=27 Participants
|
PRIMARY outcome
Timeframe: Assessed at Baseline 1 for both groups and 4 weeks later (post-intervention for intervention participants and Baseline 2 for waitlist control participants). Post-intervention data were not collected for the waitlist control group.Population: Differences between reported numbers and assigned groups reflect HRV collection challenges (e.g., self-placement difficulties, signal quality, data capture issues, and discontinuation). Usable HRV data were available for 18 intervention and 33 waitlist participants at BL1 and for 15 intervention and 36 waitlist participants at assessment 2 (waitlist participants completed a second BL assessment before intervention participation). Post-intervention HRV was not collected for the waitlist group.
Cardiovascular health was assessed using heart rate variability (HRV) measured during a socially relevant stressor task administered in each intervention session. HRV data were collected using the movisens device, a wearable chest-mounted sensor that records electrocardiogram (ECG) data. Vagally mediated HRV was calculated from the variability of inter-beat (R-R) intervals derived from these ECG recordings. Mean HRV values were calculated for each assessment period, with higher mean HRV values (per minute) indicating greater autonomic regulation and improved cardiovascular health. Due to feasibility and data quality issues with the wearable ECG device, HRV data collection was discontinued after the first two assessment periods (Baseline 1 and the 4-week assessment \[post-intervention for the intervention group/Baseline 2 for the waitlist control group\]); therefore, post-intervention HRV data were not collected for the waitlist control group.
Outcome measures
| Measure |
All Participants
n=54 Participants
For the purposes of analysis, participants from the intervention and waitlist-control arms were combined after both groups completed the intervention. All participants completed an initial baseline assessment following informed consent. Participants assigned to the intervention arm immediately received the 4-week Relational Savoring intervention. Participants assigned to the waitlist-control arm did not receive the intervention during the initial four-week period and instead completed a second baseline assessment (Baseline 2) prior to beginning the same 4-week intervention. All participants who completed the intervention subsequently completed a post-intervention assessment and a 3-month follow-up assessment.
|
Waitlist Control Group
After providing informed consent, participants assigned to the waitlist control group (n = 43) completed a baseline assessment and did not receive the intervention for the subsequent 4 weeks. At the end of this period, they completed a second baseline assessment (BL2) prior to beginning the intervention. Participants then completed additional assessments immediately post-intervention (8-weeks from enrollment) and again at a 3-month follow-up.
|
|---|---|---|
|
Impact of Intervention on Heart Rate Variability
Intervention Group Baseline 1
|
74.56 minute
Standard Deviation 10.97
|
—
|
|
Impact of Intervention on Heart Rate Variability
Intervention Group Post-Intervention
|
75.24 minute
Standard Deviation 9.87
|
—
|
|
Impact of Intervention on Heart Rate Variability
Waitlist Group Baseline 1
|
76.49 minute
Standard Deviation 9.29
|
—
|
|
Impact of Intervention on Heart Rate Variability
Waitlist Group Baseline 2
|
74.80 minute
Standard Deviation 8.91
|
—
|
PRIMARY outcome
Timeframe: Immediately following completion of the 4-week intervention and at 3 months post-intervention.Population: All participants who completed the intervention and provided information at post-intervention (n = 80) and at the 3-month follow up (n = 62).
Intervention acceptability was assessed using participant self-report items evaluating frequency of use of the intervention skills, perceived value of the intervention, willingness to recommend the intervention to others, and intention to continue engaging in the intervention skills. Acceptability was assessed only after completion of the intervention and at the 3-month follow-up. Acceptability scores were summarized using mean scores reported separately at post-intervention and at the 3-month follow-up across the sample. Possible scores ranged from 0 to 30, with higher scores indicating greater acceptability.
Outcome measures
| Measure |
All Participants
n=80 Participants
For the purposes of analysis, participants from the intervention and waitlist-control arms were combined after both groups completed the intervention. All participants completed an initial baseline assessment following informed consent. Participants assigned to the intervention arm immediately received the 4-week Relational Savoring intervention. Participants assigned to the waitlist-control arm did not receive the intervention during the initial four-week period and instead completed a second baseline assessment (Baseline 2) prior to beginning the same 4-week intervention. All participants who completed the intervention subsequently completed a post-intervention assessment and a 3-month follow-up assessment.
|
Waitlist Control Group
After providing informed consent, participants assigned to the waitlist control group (n = 43) completed a baseline assessment and did not receive the intervention for the subsequent 4 weeks. At the end of this period, they completed a second baseline assessment (BL2) prior to beginning the intervention. Participants then completed additional assessments immediately post-intervention (8-weeks from enrollment) and again at a 3-month follow-up.
|
|---|---|---|
|
Acceptability of the Relational Savoring Intervention
Post-intervention
|
24.47 Units on a scale
Standard Deviation 3.05
|
—
|
|
Acceptability of the Relational Savoring Intervention
3-month follow up
|
24.25 Units on a scale
Standard Deviation 3.03
|
—
|
PRIMARY outcome
Timeframe: Immediately before and after each weekly intervention session (Sessions 1-4, approximately 1 hour apart per session), during the 4-week intervention period.Population: Only the 80 participants (40 intervention, 40 waitlist control) who completed all four sessions of the intervention are included.
Perceived closeness to community was assessed using the Inclusion of Other in the Self-Community Version (IOS-C), a single-item visual self-report measure. Participants selected one of seven images depicting increasing overlap between two circles representing the self and the community. Greater overlap indicates greater perceived closeness to the community, whereas less overlap indicates lower perceived closeness. The measure was administered immediately before and after each intervention session (four sessions total). Scores ranged from 1 (not close at all) to 7 (very close), with higher scores indicating greater perceived closeness to the community.
Outcome measures
| Measure |
All Participants
n=80 Participants
For the purposes of analysis, participants from the intervention and waitlist-control arms were combined after both groups completed the intervention. All participants completed an initial baseline assessment following informed consent. Participants assigned to the intervention arm immediately received the 4-week Relational Savoring intervention. Participants assigned to the waitlist-control arm did not receive the intervention during the initial four-week period and instead completed a second baseline assessment (Baseline 2) prior to beginning the same 4-week intervention. All participants who completed the intervention subsequently completed a post-intervention assessment and a 3-month follow-up assessment.
|
Waitlist Control Group
After providing informed consent, participants assigned to the waitlist control group (n = 43) completed a baseline assessment and did not receive the intervention for the subsequent 4 weeks. At the end of this period, they completed a second baseline assessment (BL2) prior to beginning the intervention. Participants then completed additional assessments immediately post-intervention (8-weeks from enrollment) and again at a 3-month follow-up.
|
|---|---|---|
|
Impact of Intervention on Perceived Closeness to the Community
Post-Session 3
|
5.54 Units on a scale
Standard Error 1.49
|
—
|
|
Impact of Intervention on Perceived Closeness to the Community
Pre-Session 1
|
4.66 Units on a scale
Standard Error 1.70
|
—
|
|
Impact of Intervention on Perceived Closeness to the Community
Post-Session 1
|
5.32 Units on a scale
Standard Error 1.60
|
—
|
|
Impact of Intervention on Perceived Closeness to the Community
Pre-Session 2
|
4.76 Units on a scale
Standard Error 1.72
|
—
|
|
Impact of Intervention on Perceived Closeness to the Community
Post-Session 2
|
5.39 Units on a scale
Standard Error 1.53
|
—
|
|
Impact of Intervention on Perceived Closeness to the Community
Pre-Session 3
|
5.01 Units on a scale
Standard Error 1.71
|
—
|
|
Impact of Intervention on Perceived Closeness to the Community
Pre-Session 4
|
5.14 Units on a scale
Standard Error 1.73
|
—
|
|
Impact of Intervention on Perceived Closeness to the Community
Post-Session 4
|
5.52 Units on a scale
Standard Error 1.68
|
—
|
PRIMARY outcome
Timeframe: Immediately before and after each weekly intervention session (Sessions 1-4, approximately 1 hour apart per session), during the 4-week intervention period.Population: Only the 80 participants (40 intervention, 40 waitlist control) who completed all four sessions of the intervention are included.
Emotional valence was assessed using the valence subscale of the Self-Assessment Manikin (SAM), a nonverbal pictorial self-report measure. Participants selected one of five pictograms ranging from smiling to frowning to indicate their current emotional state. Scores ranged from 1 to 5, with lower scores indicating more positive emotional valence and higher scores indicating more negative emotional valence. The measure was administered immediately before and after each intervention session.
Outcome measures
| Measure |
All Participants
n=80 Participants
For the purposes of analysis, participants from the intervention and waitlist-control arms were combined after both groups completed the intervention. All participants completed an initial baseline assessment following informed consent. Participants assigned to the intervention arm immediately received the 4-week Relational Savoring intervention. Participants assigned to the waitlist-control arm did not receive the intervention during the initial four-week period and instead completed a second baseline assessment (Baseline 2) prior to beginning the same 4-week intervention. All participants who completed the intervention subsequently completed a post-intervention assessment and a 3-month follow-up assessment.
|
Waitlist Control Group
After providing informed consent, participants assigned to the waitlist control group (n = 43) completed a baseline assessment and did not receive the intervention for the subsequent 4 weeks. At the end of this period, they completed a second baseline assessment (BL2) prior to beginning the intervention. Participants then completed additional assessments immediately post-intervention (8-weeks from enrollment) and again at a 3-month follow-up.
|
|---|---|---|
|
Impact of Intervention on Negative Emotional Valence
Pre-session 1
|
2.05 Units on a scale
Standard Deviation 1.07
|
—
|
|
Impact of Intervention on Negative Emotional Valence
Post-session 1
|
1.35 Units on a scale
Standard Deviation 0.73
|
—
|
|
Impact of Intervention on Negative Emotional Valence
Pre-session 2
|
2.05 Units on a scale
Standard Deviation 1.04
|
—
|
|
Impact of Intervention on Negative Emotional Valence
Post-session 2
|
1.38 Units on a scale
Standard Deviation 0.65
|
—
|
|
Impact of Intervention on Negative Emotional Valence
Pre-session 3
|
1.97 Units on a scale
Standard Deviation 0.87
|
—
|
|
Impact of Intervention on Negative Emotional Valence
Post-session 3
|
1.34 Units on a scale
Standard Deviation 0.55
|
—
|
|
Impact of Intervention on Negative Emotional Valence
Pre-session 4
|
1.87 Units on a scale
Standard Deviation 0.97
|
—
|
|
Impact of Intervention on Negative Emotional Valence
Post-session 4
|
1.29 Units on a scale
Standard Deviation 0.58
|
—
|
PRIMARY outcome
Timeframe: Baseline (prior to intervention), immediately following completion of the 4-week intervention, and at 3 months post-intervention.Population: At baseline, 41 intervention participants and 43 waitlist control participants completed the assessment. At Baseline 2, only participants in the waitlist control group completed the assessment (n = 42). At post-intervention, 39 participants in the intervention group and 39 in the waitlist control group completed the assessment. At the 3-month follow-up, 31 intervention participants and 31 waitlist control participants completed the final assessment.
Sleep quality was assessed using the Pittsburgh Sleep Quality Index (PSQI), a 19-item self-report questionnaire that assesses subjective sleep quality over the past month. The PSQI yields a global sleep quality score derived from seven component scores, with total scores ranging from 0 to 21. Higher scores indicate poorer sleep quality.
Outcome measures
| Measure |
All Participants
n=41 Participants
For the purposes of analysis, participants from the intervention and waitlist-control arms were combined after both groups completed the intervention. All participants completed an initial baseline assessment following informed consent. Participants assigned to the intervention arm immediately received the 4-week Relational Savoring intervention. Participants assigned to the waitlist-control arm did not receive the intervention during the initial four-week period and instead completed a second baseline assessment (Baseline 2) prior to beginning the same 4-week intervention. All participants who completed the intervention subsequently completed a post-intervention assessment and a 3-month follow-up assessment.
|
Waitlist Control Group
n=43 Participants
After providing informed consent, participants assigned to the waitlist control group (n = 43) completed a baseline assessment and did not receive the intervention for the subsequent 4 weeks. At the end of this period, they completed a second baseline assessment (BL2) prior to beginning the intervention. Participants then completed additional assessments immediately post-intervention (8-weeks from enrollment) and again at a 3-month follow-up.
|
|---|---|---|
|
Impact of Intervention on Sleep Quality
Baseline
|
8.10 Units on a scale
Standard Deviation 3.85
|
7.73 Units on a scale
Standard Deviation 3.76
|
|
Impact of Intervention on Sleep Quality
Baseline 2
|
—
|
7.36 Units on a scale
Standard Deviation 3.19
|
|
Impact of Intervention on Sleep Quality
Post-Intervention
|
8.50 Units on a scale
Standard Deviation 3.83
|
6.91 Units on a scale
Standard Deviation 2.79
|
|
Impact of Intervention on Sleep Quality
3-month follow up
|
8.50 Units on a scale
Standard Deviation 4.47
|
8.14 Units on a scale
Standard Deviation 3.41
|
PRIMARY outcome
Timeframe: Baseline (prior to intervention), immediately following completion of the 4-week intervention, and at 3 months post-intervention.Population: At baseline, 41 intervention participants and 43 waitlist control participants completed the assessment. At Baseline 2, only participants in the waitlist control group completed the assessment (n = 42). At post-intervention, 39 participants in the intervention group and 39 in the waitlist control group completed the assessment. At the 3-month follow-up, 31 intervention participants and 31 waitlist control participants completed the final assessment.
can you revise to make it clear that scoring was dichotomized as ither true or false and thus scores ranged from: Changes in diet-related behavior were assessed using the Emotional Eating subscale of the Three-Factor Eating Questionnaire (TFEQ). The subscale consists of 3 items assessing the extent to which individuals eat in response to emotional states. Items are rated on a 4-point scale ranging from 0 (definitely true) to 3 (definitely false). Item responses were summed to create a total emotional eating score ranging from 0 to 9, with lower scores indicating greater emotional eating and higher scores indicating less emotional eating.
Outcome measures
| Measure |
All Participants
n=41 Participants
For the purposes of analysis, participants from the intervention and waitlist-control arms were combined after both groups completed the intervention. All participants completed an initial baseline assessment following informed consent. Participants assigned to the intervention arm immediately received the 4-week Relational Savoring intervention. Participants assigned to the waitlist-control arm did not receive the intervention during the initial four-week period and instead completed a second baseline assessment (Baseline 2) prior to beginning the same 4-week intervention. All participants who completed the intervention subsequently completed a post-intervention assessment and a 3-month follow-up assessment.
|
Waitlist Control Group
n=43 Participants
After providing informed consent, participants assigned to the waitlist control group (n = 43) completed a baseline assessment and did not receive the intervention for the subsequent 4 weeks. At the end of this period, they completed a second baseline assessment (BL2) prior to beginning the intervention. Participants then completed additional assessments immediately post-intervention (8-weeks from enrollment) and again at a 3-month follow-up.
|
|---|---|---|
|
Impact of Intervention on Diet
Baseline
|
2.78 Units on a scale
Standard Deviation 0.99
|
2.67 Units on a scale
Standard Deviation 0.96
|
|
Impact of Intervention on Diet
Baseline 2
|
—
|
2.32 Units on a scale
Standard Deviation 0.98
|
|
Impact of Intervention on Diet
Post-intervention
|
2.44 Units on a scale
Standard Deviation 0.92
|
2.24 Units on a scale
Standard Deviation 1.07
|
|
Impact of Intervention on Diet
3-month follow up
|
2.28 Units on a scale
Standard Deviation 0.99
|
2.09 Units on a scale
Standard Deviation 0.99
|
PRIMARY outcome
Timeframe: From baseline (prior to intervention), immediately following completion of the 4-week intervention, and at 3 months post-intervention.Population: At baseline, 41 intervention participants and 43 waitlist control participants completed the assessment. At Baseline 2, only participants in the waitlist control group completed the assessment (n = 42). At post-intervention, 39 participants in the intervention group and 39 in the waitlist control group completed the assessment. At the 3-month follow-up, 31 intervention participants and 31 waitlist control participants completed the final assessment.
Burnout related to the COVID-19 pandemic was assessed using the COVID-19 Burnout Scale, a 10-item self-report measure. Items assess feelings of emotional exhaustion and hopelessness related to the pandemic and are rated on a 7-point scale ranging from 0 (never) to 6 (all the time). Item responses are summed to create a total burnout score ranging from 0 to 60, with higher scores indicating greater burnout. The measure was administered at baseline (1 and 2), post-intervention, and at the 3-month follow-up.
Outcome measures
| Measure |
All Participants
n=41 Participants
For the purposes of analysis, participants from the intervention and waitlist-control arms were combined after both groups completed the intervention. All participants completed an initial baseline assessment following informed consent. Participants assigned to the intervention arm immediately received the 4-week Relational Savoring intervention. Participants assigned to the waitlist-control arm did not receive the intervention during the initial four-week period and instead completed a second baseline assessment (Baseline 2) prior to beginning the same 4-week intervention. All participants who completed the intervention subsequently completed a post-intervention assessment and a 3-month follow-up assessment.
|
Waitlist Control Group
n=43 Participants
After providing informed consent, participants assigned to the waitlist control group (n = 43) completed a baseline assessment and did not receive the intervention for the subsequent 4 weeks. At the end of this period, they completed a second baseline assessment (BL2) prior to beginning the intervention. Participants then completed additional assessments immediately post-intervention (8-weeks from enrollment) and again at a 3-month follow-up.
|
|---|---|---|
|
Impact of Intervention on Burnout
3-month follow-up
|
18.00 Units on a scale
Standard Deviation 8.25
|
15.50 Units on a scale
Standard Deviation 7.51
|
|
Impact of Intervention on Burnout
Baseline
|
19.20 Units on a scale
Standard Deviation 11.52
|
22.13 Units on a scale
Standard Deviation 13.65
|
|
Impact of Intervention on Burnout
Baseline 2
|
—
|
16.54 Units on a scale
Standard Deviation 8.39
|
|
Impact of Intervention on Burnout
Post-Intervention
|
18.82 Units on a scale
Standard Deviation 10.21
|
14.69 Units on a scale
Standard Deviation 7.68
|
PRIMARY outcome
Timeframe: From baseline (prior to intervention), immediately following completion of the 4-week intervention, and at 3 months post-intervention.Population: At baseline, 41 intervention participants and 43 waitlist control participants completed the assessment. At Baseline 2, only participants in the waitlist control group completed the assessment (n = 42). At post-intervention, 39 participants in the intervention group and 39 in the waitlist control group completed the assessment. At the 3-month follow-up, 31 intervention participants and 31 waitlist control participants completed the final assessment.
Job satisfaction was assessed using the Job Satisfaction Scale, a 36-item self-report questionnaire measuring participants' overall attitudes toward their job. Items were rated on a 6-point Likert-type scale ranging from 1 (disagree very much) to 6 (agree very much). Item responses were summed to create a total job satisfaction score ranging from 36 to 216, with higher scores indicating greater job satisfaction. The measure was administered at baseline (1 and 2), post-intervention, and at the 3-month follow-up.
Outcome measures
| Measure |
All Participants
n=41 Participants
For the purposes of analysis, participants from the intervention and waitlist-control arms were combined after both groups completed the intervention. All participants completed an initial baseline assessment following informed consent. Participants assigned to the intervention arm immediately received the 4-week Relational Savoring intervention. Participants assigned to the waitlist-control arm did not receive the intervention during the initial four-week period and instead completed a second baseline assessment (Baseline 2) prior to beginning the same 4-week intervention. All participants who completed the intervention subsequently completed a post-intervention assessment and a 3-month follow-up assessment.
|
Waitlist Control Group
n=43 Participants
After providing informed consent, participants assigned to the waitlist control group (n = 43) completed a baseline assessment and did not receive the intervention for the subsequent 4 weeks. At the end of this period, they completed a second baseline assessment (BL2) prior to beginning the intervention. Participants then completed additional assessments immediately post-intervention (8-weeks from enrollment) and again at a 3-month follow-up.
|
|---|---|---|
|
Impact of Intervention on Job Satisfaction
Baseline
|
140.78 Units on a scale
Standard Deviation 18.83
|
141.45 Units on a scale
Standard Deviation 20.12
|
|
Impact of Intervention on Job Satisfaction
Baseline 2
|
—
|
141.67 Units on a scale
Standard Deviation 21.41
|
|
Impact of Intervention on Job Satisfaction
Post-intervention
|
139.47 Units on a scale
Standard Deviation 16.81
|
142.81 Units on a scale
Standard Deviation 19.77
|
|
Impact of Intervention on Job Satisfaction
3-month follow up
|
140.37 Units on a scale
Standard Deviation 14.94
|
147.28 Units on a scale
Standard Deviation 20.07
|
PRIMARY outcome
Timeframe: From baseline (prior to intervention), immediately following completion of the 4-week intervention, and at 3 months post-intervention.Population: At baseline, 41 intervention participants and 43 waitlist control participants completed the assessment. At Baseline 2, only participants in the waitlist control group completed the assessment (n = 42). At post-intervention, 39 participants in the intervention group and 39 in the waitlist control group completed the assessment. At the 3-month follow-up, 31 intervention participants and 31 waitlist control participants completed the final assessment.
Psychological distress was assessed using the Brief Symptom Inventory (BSI), a 19-item self-report measure assessing symptoms of depression, anxiety, and somatic distress. Items were rated on a 6-point scale ranging from 0 (not at all) to 5 (extremely). Item responses were summed to create a global psychological distress score ranging from 0 to 95, with higher scores indicating greater overall distress. The measure was administered at baseline (1 and 2), post-intervention, and at the 3-month follow-up.
Outcome measures
| Measure |
All Participants
n=41 Participants
For the purposes of analysis, participants from the intervention and waitlist-control arms were combined after both groups completed the intervention. All participants completed an initial baseline assessment following informed consent. Participants assigned to the intervention arm immediately received the 4-week Relational Savoring intervention. Participants assigned to the waitlist-control arm did not receive the intervention during the initial four-week period and instead completed a second baseline assessment (Baseline 2) prior to beginning the same 4-week intervention. All participants who completed the intervention subsequently completed a post-intervention assessment and a 3-month follow-up assessment.
|
Waitlist Control Group
n=43 Participants
After providing informed consent, participants assigned to the waitlist control group (n = 43) completed a baseline assessment and did not receive the intervention for the subsequent 4 weeks. At the end of this period, they completed a second baseline assessment (BL2) prior to beginning the intervention. Participants then completed additional assessments immediately post-intervention (8-weeks from enrollment) and again at a 3-month follow-up.
|
|---|---|---|
|
Impact of Intervention on Psychological Distress
Baseline
|
13.24 Units on a scale
Standard Deviation 13.03
|
9.60 Units on a scale
Standard Deviation 8.59
|
|
Impact of Intervention on Psychological Distress
Baseline 2
|
—
|
8.62 Units on a scale
Standard Deviation 7.65
|
|
Impact of Intervention on Psychological Distress
Post-intervention
|
11.19 Units on a scale
Standard Deviation 14.16
|
8.31 Units on a scale
Standard Deviation 8.28
|
|
Impact of Intervention on Psychological Distress
3-month follow up
|
11.37 Units on a scale
Standard Deviation 10.38
|
6.57 Units on a scale
Standard Deviation 6.84
|
PRIMARY outcome
Timeframe: From baseline (prior to intervention), immediately following completion of the 4-week intervention, and at 3 months post-intervention.Population: At baseline, 41 intervention participants and 43 waitlist control participants completed the assessment. At Baseline 2, only participants in the waitlist control group completed the assessment (n = 42). At post-intervention, 39 participants in the intervention group and 39 in the waitlist control group completed the assessment. At the 3-month follow-up, 31 intervention participants and 31 waitlist control participants completed the final assessment.
General health was assessed using the General Health subscale of the Short Form Health Survey (SF-36). Participants completed the full SF-36 questionnaire, and the 5 items comprising the General Health subscale were scored according to standard SF-36 procedures. Item responses were recoded and summed, and the raw subscale score was transformed to a 0-100 scale, with higher scores indicating better perceived physical health. The measure was administered at baseline (1 and 2), post-intervention, and at the 3-month follow-up.
Outcome measures
| Measure |
All Participants
n=41 Participants
For the purposes of analysis, participants from the intervention and waitlist-control arms were combined after both groups completed the intervention. All participants completed an initial baseline assessment following informed consent. Participants assigned to the intervention arm immediately received the 4-week Relational Savoring intervention. Participants assigned to the waitlist-control arm did not receive the intervention during the initial four-week period and instead completed a second baseline assessment (Baseline 2) prior to beginning the same 4-week intervention. All participants who completed the intervention subsequently completed a post-intervention assessment and a 3-month follow-up assessment.
|
Waitlist Control Group
n=43 Participants
After providing informed consent, participants assigned to the waitlist control group (n = 43) completed a baseline assessment and did not receive the intervention for the subsequent 4 weeks. At the end of this period, they completed a second baseline assessment (BL2) prior to beginning the intervention. Participants then completed additional assessments immediately post-intervention (8-weeks from enrollment) and again at a 3-month follow-up.
|
|---|---|---|
|
Impact of Intervention on General Health
Baseline
|
53.51 Units on a scale
Standard Deviation 20.67
|
57.13 Units on a scale
Standard Deviation 18.41
|
|
Impact of Intervention on General Health
Baseline 2
|
—
|
58.43 Units on a scale
Standard Deviation 14.54
|
|
Impact of Intervention on General Health
Post-intervention
|
56.10 Units on a scale
Standard Deviation 20.35
|
59.03 Units on a scale
Standard Deviation 15.58
|
|
Impact of Intervention on General Health
3-month follow up
|
54.67 Units on a scale
Standard Deviation 17.66
|
59.53 Units on a scale
Standard Deviation 15.21
|
PRIMARY outcome
Timeframe: Baseline (prior to intervention), immediately following completion of the 4-week intervention, and at 3 months post-intervention.Population: No data were collected for this outcome due to logistical challenges experienced by community partners. Specifically, each participating agency used different methods for documenting engagement by community health workers, and harmonizing these procedures to capture comparable data was not feasible. Given these constraints, this outcome was not collected and will not be collected in the future.
Community outreach was assessed using a composite measure of community engagement and reach in community health programming. The composite index captured the extent to which community members were reached by community health programming and was calculated using four indicators: (1) number of days community service providers (CSPs) worked, (2) number of health-related events offered by CSPs, (3) community attendance at CSP-led events, and (4) retention of community members across multi-day programs. Indicators were combined to create a total community outreach score, with higher scores reflecting greater outreach and a higher number of community members reached through community health programming.
Outcome measures
Outcome data not reported
Adverse Events
Intervention Group
Waitlist Control Group
Serious adverse events
Adverse event data not reported
Other adverse events
Adverse event data not reported
Additional Information
Results disclosure agreements
- Principal investigator is a sponsor employee
- Publication restrictions are in place