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Enhancing Emotional and Motivational Development to Support Well-being and Retention in Diverse University Students

University of Arizona logo

University of Arizona

Status

Completed

Conditions

Healthy

Treatments

Behavioral: Placebo
Behavioral: Contextualized Wish-Outcome-Obstacle-Plan (WOOP) intervention

Study type

Interventional

Funder types

Other

Identifiers

NCT05294913
2104695049

Details and patient eligibility

About

Higher education is crucial for young adults in their intake of knowledge and skills to further their careers and reach their potentials. However, going through college is not necessarily an easy path. The purpose of this study is to enhance university students' well-being and educational experience by examining factors associated with stress and well-being.

The investigator plans to recruit eighty participants from a large public university in the US to provide survey data and saliva samples at two waves during the data collection semester (beginning and end of the semester). Survey data will include demographic information and help gauge psychosocial factors related to stress and well-being. Saliva will be tested for two biomarkers each wave of data collection, cortisol (sampling three times a day for diurnal patterns for two consecutive days) and c-reactive protein, which indicate physiological stress/immune responses. Additionally, participants be randomly assigned to an intervention (n = 40) or control group (n = 40), where the intervention group will undertake a brief intervention focused on motivation and emotion regulation circa mid-semester and the control group will receive a placebo goal-setting short training. The investigator aims to examine whether intervention efforts can enhance end-of-semester psychological and physiological well-being, and particularly, whether students from diverse backgrounds (e.g., first-generation, low-income, and/or BIPOC) can benefit from the intervention.

The investigator will use advanced quantitative data analysis (using Mplus v.8, in a structural equation modeling framework) to examine intervention efficacy and group differences. The investigator hypothesizes that those receiving the intervention will display a healthier profile at the end of the semester compared to their control group counterparts; and the investigator hypothesize students from diverse backgrounds will have significantly improved results from the intervention.

The study will allow a better understanding to crucial steps towards exploring how to improve the well-being, higher-education pipeline, and retention of students with diverse backgrounds, providing insight on how each student's university experience can be improved.

Enrollment

39 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • participants who are currently enrolled students at a large public university in the Southwest of US.

Exclusion criteria

  • individuals below the age of 18 or those who are not currently enrolled students at said university.

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

39 participants in 2 patient groups, including a placebo group

Intervention group
Experimental group
Treatment:
Behavioral: Contextualized Wish-Outcome-Obstacle-Plan (WOOP) intervention
Placebo control group
Placebo Comparator group
Treatment:
Behavioral: Placebo

Trial contacts and locations

1

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Central trial contact

Katherine C Cheng, PhD

Data sourced from clinicaltrials.gov

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