Skip to content

Community Health Through Engagement and Environmental Renewal

Community Health Through Engagement and Environmental Renewal

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04362475
Acronym
CHEER
Enrollment
915
Registered
2020-04-27
Start date
2021-05-21
Completion date
2025-09-01
Last updated
2026-03-13

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

Conditions

Blight, Family Relations

Brief summary

Community Health from Engagement and Environmental Renewal (CHEER) will leverage previous Centers for Disease Control and Prevention (CDC) community engagement projects to reach and intervene on a high need population. Disadvantage and poverty have long-term and transgenerational adverse impacts on social interaction and cohesion and residents' emotional and physical health. Mothers living and raising children in these conditions face multiple stressors without the community support previous generations relied on. Decades of research on American cities have connected the social, economic, and physical characteristics of neighborhoods with a lack of social cohesion, inability to maintain shared norms of acceptable behavior,and increases in health disparities and risky behaviors. Social cohesion and collective efficacy inversely associate with depression among youth. In a parallel manner, improved parenting practices and youth behavior directly associate with neighborhood social interactions and social cohesion. While these associations are suggestive, CHEER will directly test causal hypotheses at the neighborhood and family levels in a randomized control trial, that can significantly advance the evidence base for public health interventions: Family Youth Intervention (FYI) and an Environment: Social and Physical Intervention (ESPI) to increase social interaction, social cohesion, and collective efficacy and influence wellbeing of mothers and their youth.

Detailed description

Aim 1 Family System: To test the effect of FYI on primary outcomes of youth psychosocial behaviors and sexual risk compared to a Wait List Control. 1a. FYI will significantly improve our primary outcomes of externalizing (e.g. impulsivity, violence, theft) and internalizing (e.g. depression, withdrawal, anxiety, loneliness) behaviors and early and risky sex (i.e. sexual initiation at less than 16 years of age and sexual intercourse without a condom) (Effectiveness). 1. b. FYI will significantly lower parental stress, improve maternal emotional health, enhance parenting skills and improve youth Social and Emotional Competence (SEC) to change primary outcomes (Mediation). Aim 2 Community System: To test the effect of ESPI on neighborhood environment compared to Wait List Control. 2. a. ESPI significantly will increase our primary outcomes of social interaction, social cohesion, collective efficacy, and shared norms compared to wait list control (Effectiveness). 2b. Engaging residents in community-designed and -led projects to develop common spaces will significantly improve neighborhood perceptions (e.g. attractiveness, safety) and provide opportunities for residents to interact to change primary outcomes (Mediation). Aim 3 Community and Family Systems: To test the effects of combining FYI and ESPI on the same youth and neighborhood environmental outcomes as in Aims 1 and 2 compared to FYI alone, ESPI alone, and a Wait List Control. 3a. ESPI and FYI will significantly reduce primary youth and neighborhood environmental outcomes (Effectiveness). 3b. ESPI and FYI will change neighborhood environmental and family processes to change primary outcomes of adolescent SEC, external and internal behaviors, and early and risky sex (Mediation).

Interventions

BEHAVIORALCommunity Health through Engagement and Environmental Renewal (CHEER)

FYI and ESPI intervention activities will be implemented in the overall study, CHEER. It will also allow us to examine possible synergistic effects of both interventions when implemented in the same neighborhoods. Separate sets of participants will be selected for the FYI comparisons and for the ESPI comparisons. Because the FYI intervention focuses on mothers and their children, participants for the FYI comparisons will be selected by Respondent Driven Sampling of eligible families from the neighborhoods in all four cells. The ESPI intervention targets the whole neighborhood, and thus a random sample of neighborhood residents will be enrolled in each of the four cells. Because the primary outcomes for FYI and ESPI are connected but differ from each other, the FYI samples will be assessed for the FYI outcomes in all four cells and the ESPI samples will be assessed for the ESPI outcomes in all four cells.

Sponsors

University of Alabama at Birmingham
Lead SponsorOTHER
Centers for Disease Control and Prevention
CollaboratorFED

Study design

Allocation
RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
PREVENTION
Masking
NONE

Intervention model description

Hypotheses will be tested in a 2 X 2 design that includes the independent and combined effects of two interventions targeting the individual, family, and community level. Participating neighborhoods will be assigned into one of four cells: FYI alone, ESPI alone, FYI and ESPI combined, and Wait List Control.

Eligibility

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

Inclusion criteria

* For FYI, parents who reside in the FYI intervention neighborhood (North Titusville, South Titusville, Rising -West Princeton, and Belview Heights) and have a child age 11-16 years. * For ESPI, residents who live in the ESPI intervention neighborhoods (North Titusville, South Titusville, Druid Hills, and Fountain Heights).

Exclusion criteria

* For FYI, does not met the above requirements and did not consent to participate. * For ESPI, not residing in one of the above neighborhoods and did not consent to participate.

Design outcomes

Primary

MeasureTime frameDescription
Number of Participants Who Like Living in Their NeighborhoodBaselineSurvey item on whether they like or dislike living their neighborhood.
Problem Behaviors in Children Ages 11 to 16 Years.Baseline, 1-week and 6-month Follow-upThree items asked have the child ever been suspended from school and within the past 12 months prior to the baseline survey have they smoked cigarettes or drunk alcohol. Participants choose 1 for yes and 0 for no. The range is form 0 to 3, where 3 describes a higher problematic behavior. Three questions were asked at 1-week and 6 month follow-up: have they been suspended from school, smoked cigarettes or drunk alcohol since baseline.
Age of Sexual InitiationBaselineYear of age at sex. Two variables were used to measure sexual initiation. Answer choices ranged continuously from 1 (10 years old) to 9 (18 years or older).
Number of Participants Who Participates in Risky SexBaselineFollow-up questions for individuals endorsing sexual initiation to assess risky sex behavior. The count was assessed on how often did the participant had sex without a condom.
Project on Human Development in Chicago Neighborhoods: Community Survey- Cohesion Index SubscaleBaseline, 12-month Follow up 1 and 18-month Follow up 2Project on Human Development in Chicago Neighborhoods: Community Survey assesses city-level variables relating to neighborhood structure. This scale consisted of 7 items that were measured on a scale of 1 to 6. The range of scores are from 7 to 35. The mean score was analyzed where the higher the score the community interaction was the worst.
Project on Human Development in Chicago Neighborhoods: Community Survey- Neighborhood PerceptionBaseline, 12-month Follow up and 18-month Follow-upProject on Human Development in Chicago Neighborhoods: Community Survey assesses city-level variables relating to neighborhood structure. Three items on a scale of 1 to 6, were used to measure how participants perceive their neighborhood. The range of the scores were from 3 to 12. The mean score was analyzed where the higher the score is a better overall perception of their neighborhood.
Social Contacts and Resources ScaleBaseline, 12- month Follow up 1, and 18-month Follow up 2Social Contacts and Resources Scale, a 5-item measure of social activities with their neighbors. Responses ranged from 1 (never) to 4 (often). a total mean score were derived where higher scores indicating greater social contact. The scores range from 5 to 20.

Secondary

MeasureTime frameDescription
Parent-Adolescent CommunicationBaseline, 1-week and 6-month follow upThis is a 20-item scale where response choices range from 1= Strongly Disagree to 5= Strongly Agree. Items are summed to arrive at a total communication score (range 20-100), with higher scores suggesting better overall communication quality.
Parental NurturanceBaseline, 1-week and 6-month follow upMeasured using using a single item, " I get the emotional help and support I need from my family." The responses to the item is on a 7-point likert scale ranging from Very Strongly Agree to Very Strongly Disagree where Very Strongly Disagree describes a less nurturing parent and Very Strongly Agree describes more nurturance the parent displays. Scores ranged from 1 to 7.
Family FunctioningBaseline, 1-week and 6-month follow upAmerican Strength Inventory was uses six categories to measure the strength of a family. Participants responded with Not true (1), Sometimes true (2) and Often true (3). The items were added for a total family strength score where a mean score was analyzed. The subscale Global Measure was used to measure family functioning. The scores range from 4 to 12, where the higher the score the higher the family functioning.
CopingBaseline, 1-week and 6-month follow upMeasured using the Managing Stress and Crisis Effectively subscale of the American Family Strength Inventory assess family functioning and qualities that makes a family strong. Participants responded with Not true (1), Sometimes true (2) and Often true (3). The scores ranged from 6 to 24. The items were added for a total family strength score where a mean score was analyzed. Higher mean scores means higher coping with stress skills.
Perceived DepressionBaseline, 1-week and 6-month follow upThe Patient Health Questionnaire Scale (PHQ-9) is a abbreviated scale that measures self-report depressive symptoms. Respondents report on a 4-point likert scale where 0 is Not at All and 3 is Nearly Everyday. Items were added to determine the presence and severity of depressive symptoms. The range of the scores are 0 to 27. Score interpretations are 1-4 Minimal depression, 5-9 Mild depression, 10-14 Moderate depression,15-19 Moderately severe depression, and 20-27 Severe depression. A mean score was analyzed.
Social SupportBaseline, 1-week and 6-month follow upMeasured using items from the World Health Organization's Quality of Life Questionnaire to measure satisfaction with the level of social support they receive. The responses were on a 5-point likert scale ranging from very dissatisfied (1) to very satisfied (5). The higher the score the more scarification with their social support.
The World Health Organization Quality of Life Brief ScaleBaseline, 1-week and 6-month follow upThe World Health Organization Quality of Life Brief Scale measures four domains of quality of life: physical health, psychological, social relations and environment. The scores are transformed on a scale from 0 to 100 where higher score mean higher quality of life.
Punitive Discipline ScaleBaseline, 1-week and 6-month follow upPunitive discipline is assessed using four items that indicate the frequency of spanking/hitting, scolding, and threatening to spank/hit or threatening to punish. Response categories included 1 = never in past 12 months; 2 = a few times; 3 = once a month or more; 4 = once a week or more; and, 5 = almost everyday. After totaling the score, the higher the score the more the parent uses punitive discipline. Scores range from 4 to 20 where the higher the score the more often the parent used punitive discipline. A mean score was analyzed.
Parental Monitoring ScaleBaseline, 1-week and 6-month follow upAdolescents reported how often their parents knew where they were and what they were doing after school, on weeknights, and on weekends. All items used a 4-point scale ranging from 1 (almost never), to 2 (sometimes), to 3 (usually), to 4 (almost always). Scores ranging from 1 (low levels of parental monitoring) to 4 (high levels of parental monitoring). The range of the scores are 7-28. After totaling the score, the higher the score the higher levels of parental monitoring were present. A mean score was analyzed.

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORJeff T Walker, PhD

University of Alabama at Birmingham

Baseline characteristics

Characteristic
Age, Continuous52 years
STANDARD_DEVIATION 20
Birmingham United Neighborhood (BUN)92 Participants
How long live in neighborhood
11 to 20 years
63 Participants
How long live in neighborhood
1 to 5 years
87 Participants
How long live in neighborhood
6 to 10 years
45 Participants
How long live in neighborhood
Less than a Year
5 Participants
How long live in neighborhood
Over 20 years
41 Participants
How long live in neighborhood
Unknown
6 Participants
Neighborhood
Belview Heights
23 Participants
Neighborhood
Druid Hills
57 Participants
Neighborhood
Fountain Heights
6 Participants
Neighborhood
North Titusville
8 Participants
Neighborhood
Other
108 Participants
Neighborhood
Riley Travellick
50 Participants
Neighborhood
Rising West Princeton
43 Participants
Neighborhood
South Titusville
89 Participants
Neighborhood
Unknown
0 Participants
Neighborhood
West Goldwire
18 Participants
Plan to Move
No
133 Participants
Plan to Move
Unknown
1 Participants
Plan to Move
Yes
50 Participants
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants
Race (NIH/OMB)
Asian
0 Participants
Race (NIH/OMB)
Black or African American
222 Participants
Race (NIH/OMB)
More than one race
10 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants
Race (NIH/OMB)
Unknown or Not Reported
6 Participants
Race (NIH/OMB)
White
8 Participants
Region of Enrollment
United States
237 participants
Sex: Female, Male
Sex/Gender
Female
87 Participants
Sex: Female, Male
Sex/Gender
Male
39 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
EG002
affected / at risk
deaths
Total, all-cause mortality
0 / 2370 / 2000 / 280
other
Total, other adverse events
0 / 2370 / 2000 / 280
serious
Total, serious adverse events
0 / 2370 / 2000 / 280

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 14, 2026