Skip to content

Evaluating a Digital Peer Mentoring Platform With College Student Populations

Evaluating the Acceptability, Feasibility, and Efficacy of a Digital Peer Mentoring Platform With College Student Populations

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05764785
Enrollment
63
Registered
2023-03-13
Start date
2023-06-22
Completion date
2023-08-21
Last updated
2023-10-12

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

Conditions

Anxiety, Depression, Mentoring to Support the Transition to College, Well-Being, Psychological

Brief summary

The goal of this clinical trial is to test the acceptability, feasibility, and efficacy of MentorPRO, a novel application that connects mentors and mentees, among incoming college first-year students in a public university. The main questions it aims to answer are: * What is the acceptability and feasibility of the MentorPRO mentoring platform? * Does mentoring with MentorPRO demonstrate an impact on academic outcomes (i.e., GPA) and indices of wellbeing (i.e., mental health, connectedness, academic self-efficacy, and overall wellbeing) among a diverse sample of incoming or first year college students? Participants in the MentorPRO group will: * Use MentorPRO with their assigned mentors to communicate for 9 weeks about transitioning to college and completing a brief summer course at the university * Complete surveys about their opinions of MentorPRO All participants (regardless of group assignment) will: * Complete surveys about their mental health and overall wellbeing * Work with a mentor throughout participation in a brief summer course at the university

Detailed description

Every student in the identified program this summer (and meets the study eligibility criteria) will be eligible to participate in the study. Students who opt into participation in research activities will complete two brief surveys. Students in the intervention condition will use MentorPRO, which is a novel application and web platform for mentoring programs that allows students to set goals, track their challenges, and find just-in time resources, while connecting to a mentor for personalized support and progress monitoring. All students in in the program will be matched with a peer mentor. Students will be assigned to mentoring using MentorPRO (intervention condition) or as-usual (control condition) based on the timing of their courses; students in the morning courses and virtual courses of the summer program will use MentorPRO. All students involved in the summer program will be involved in one week of orientation, six weeks of academic programming and peer mentoring (June 12th-July 21st), meeting four days per week during the summer prior to mentees' first year in college, as well as two weeks of post-program peer mentoring (total trial of nine weeks). At the beginning of their membership with the program, all students and mentors will be invited to participate in additional research activities. Recruitment invitations will be in postcard format from Dr. Jean Rhodes or from program staff, explaining what the study is about, what is involved for participants, what the eligibility criteria is, and a link to a Qualtrics form. The Qualtrics link will have (in order): an informed consent, an eligibility screener, and if eligible, and the pre-intervention survey (Time 1; T1). Program leaders will also promote the research project during program time, in which staff will use the same language provided in the recruitment email and flier. Students will also have time to ask questions, and any questions in which program staff cannot answer will be escalated to the research team. Individuals will also be provided the contact information of the study Principal Investigator (Dr. Jean Rhodes) in the consent form so that they can ask any questions before consenting, if relevant. Student mentees: All interested participants will let us know their age (to determine whether they complete an informed consent or their parent/guardian completes the informed consent), and then will read and sign an informed consent, after having time to ask questions to program staff and the research team. Then, they will complete an eligibility screener, and if eligible will complete the rest of the baseline survey. Interested and eligible participants will then be prompted to take the pre-intervention survey after consenting to the study (T1). All students consenting to participate will be assigned to a peer mentor in the program. Each peer mentor will be assigned to provide mentoring as usual (without MentorPRO) or provide mentoring via MentorPRO. Students will complete the summer course for 6 weeks following a week of orientation, and will receive peer mentoring during that time. For two weeks after the course, students will be able to contact their peer mentor with questions. At the end of the 9-week trial, students will receive a final survey (T2). The eligibility screener, informed consent, and the surveys will be administered via a Qualtrics link. At the conclusion of their participation, all participants will receive a debriefing statement explaining the study and where to find additional resources if needed. Intervention condition: In addition to the training in program policies and relationship building provided to program peer mentors, mentors in the MentorHub UMB group will undergo training designed by the research team. Mentors will complete a brief (30-min) online videos and orientation to the MentorHub UMB technology, followed by a 30-min interactive online course on providing supportive accountability, through MentorHub UMB Academy which includes knowledge checks to ensure mentors are engaged and understanding the material and tracks progress to ensure course completion. Additional courses will be available to mentors through the academy, including a course on mentoring ethics. Following the online training, groups of mentors will engage in a live web-conference (zoom) session with at least one staff member from UMB and at least one member of the research team, who will use motivational interviewing techniques to ensure mentor buy-in and engagement and review content from the online training modules with mentors. Finally, mentees will be given access to an online orientation to MentorHub UMB, which walks them through instructions about how to download and use the app. All study participants (mentors and student mentees) will have access to tech support within 24 hours from Academic Web Pages for any questions or issues that arise. Mentors in the intervention condition may recommend students to use a third-party mental health app (Healthy Minds Program; HMP) if needed and provide supportive accountability (i.e., encouragement, nudges, etc) to promote consistent active engagement with HMP. Data on students' engagement with HMP will be provided at the end of the trial from the Healthy Minds team (exported from Amazon Web Services by the research team). Mentors will be encouraged provide weekly supportive accountability to students using Healthy Minds. Mentors: At the end of the summer program, mentors will be recruited to complete a survey. Interested mentors will fill out an eligibility screener, and, if eligible, an informed consent form and brief demographics survey (all through Qualtrics), and survey with asking about their experiences as a mentor.

Interventions

BEHAVIORALMentorPRO

MentorPRO is a novel application and web platform for mentoring programs that allows students to set goals, track their challenges, and find just-in time resources, while connecting to a mentor for personalized support and progress monitoring.

Sponsors

University of Massachusetts, Boston
CollaboratorOTHER
National Institute of Mental Health (NIMH)
CollaboratorNIH
Academic Web Pages
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Masking description

Participants will know which condition they are assigned (mentors will know if they are using MentorPRO; students will know if they are using MentorPRO). Researchers will also know participant group allocation.

Intervention model description

Participants assigned based on the timing of their courses in the summer program

Eligibility

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

Inclusion criteria

* Being a current member of the identified summer program (Directions for Student Potential at the University of Massachusetts Boston during the 2023 summer) * Can speak, read, and write in English * Has access to a smartphone * 18-years-old or older * Any self-reported symptoms of anxiety, depression, life dissatisfaction, or lack of college belonging

Exclusion criteria

* Not a member of the identified summer program (Directions for Student Potential at the University of Massachusetts Boston during the 2023 summer) * No access to smartphone * Cannot speak, read, and write in English * under 18-years-old * Not reporting any symptoms of anxiety, depression, life dissatisfaction, or lack of college belonging

Design outcomes

Primary

MeasureTime frameDescription
Self-reported Anxiety Symptoms9 weeks after program startGeneral Anxiety Disorder - 7 (GAD-7): Anxiety symptoms over the last two weeks Scores range from 0 (no anxiety symptoms) to 21 (extreme/severe anxiety symptoms)
Self-reported Depression Symptoms9 weeks after program startPatient Health Questionnaire - 9 (PHQ-9): Depression symptoms over the last two weeks, minus item 9 (suicidal ideation) Scores range from 0 (no depression symptoms) to 24 (high/extreme depression symptoms).
Life Satisfaction9 weeks after program startSingle item of current life satisfaction: In general, how satisfied are you with your life? Responses ranging from 1 (very satisfied) to 4 (very dissatisfied)

Secondary

MeasureTime frameDescription
Academic Self-efficacy9 weeks after program startSingle item of feelings of academic self-efficacy: I am confident that I will be a successful student at UMass Boston. Scores range from strongly disagree (1) to strongly agree (5) Greater scores reflect greater perceived academic self-efficacy
Cognitive Load9 weeks after program startSingle item assessing cognitive load of finding resources on campus: It can be exhausting to find the information and resources I need to succeed. Scores range from strongly disagree (1) to strongly agree (5) Greater scores reflect greater perceived exhaustion when finding needed resources
Sense of Belonging to the University Community9 weeks after program startSingle item assessing feelings of sense of belonging: I feel part of the UMass Boston community. Scores range from strongly disagree (1) to strongly agree (5) Greater scores reflect greater sense of belonging to the university community

Countries

United States

Participant flow

Pre-assignment details

All participants were assigned to their conditions at enrollment.

Participants by arm

ArmCount
MentorPRO
Participants assigned to use MentorPRO MentorPRO: MentorPRO is a novel application and web platform for mentoring programs that allows students to set goals, track their challenges, and find just-in time resources, while connecting to a mentor for personalized support and progress monitoring.
25
Control
Participants in mentoring program as usual
38
Total63

Baseline characteristics

CharacteristicMentorPROControlTotal
Academic self-efficacy4.04 units on a scale
STANDARD_DEVIATION 1.04
4.39 units on a scale
STANDARD_DEVIATION 0.79
4.26 units on a scale
STANDARD_DEVIATION 0.9
Age, Categorical
<=18 years
0 Participants0 Participants0 Participants
Age, Categorical
>=65 years
0 Participants0 Participants0 Participants
Age, Categorical
Between 18 and 65 years
25 Participants38 Participants63 Participants
Age, Continuous18.36 years
STANDARD_DEVIATION 0.7
18.11 years
STANDARD_DEVIATION 0.39
18.21 years
STANDARD_DEVIATION 0.55
Ethnicity (NIH/OMB)
Hispanic or Latino
12 Participants18 Participants30 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
10 Participants18 Participants28 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
3 Participants2 Participants5 Participants
Life satisfaction1.83 units on a scale
STANDARD_DEVIATION 0.82
2.13 units on a scale
STANDARD_DEVIATION 0.96
2.02 units on a scale
STANDARD_DEVIATION 0.91
Perceived cognitive load2.88 units on a scale
STANDARD_DEVIATION 1.17
2.76 units on a scale
STANDARD_DEVIATION 1
2.81 units on a scale
STANDARD_DEVIATION 1.06
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Asian
6 Participants1 Participants7 Participants
Race (NIH/OMB)
Black or African American
12 Participants12 Participants24 Participants
Race (NIH/OMB)
More than one race
2 Participants2 Participants4 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Unknown or Not Reported
4 Participants10 Participants14 Participants
Race (NIH/OMB)
White
1 Participants13 Participants14 Participants
Region of Enrollment
United States
25 participants38 participants63 participants
Self-reported anxiety symptoms6.36 units on a scale
STANDARD_DEVIATION 5.74
4.13 units on a scale
STANDARD_DEVIATION 5.2
5.02 units on a scale
STANDARD_DEVIATION 5.48
Self-reported depression symptoms7.28 units on a scale
STANDARD_DEVIATION 5.81
5.76 units on a scale
STANDARD_DEVIATION 4.21
6.37 units on a scale
STANDARD_DEVIATION 4.92
Sense of belonging to university3.76 units on a scale
STANDARD_DEVIATION 1.01
3.95 units on a scale
STANDARD_DEVIATION 1.09
3.87 units on a scale
STANDARD_DEVIATION 1.05
Sex/Gender, Customized
Female
13 Participants19 Participants32 Participants
Sex/Gender, Customized
Male
11 Participants18 Participants29 Participants
Sex/Gender, Customized
Non-binary
1 Participants1 Participants2 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 230 / 30
other
Total, other adverse events
0 / 230 / 30
serious
Total, serious adverse events
0 / 230 / 30

Outcome results

Primary

Life Satisfaction

Single item of current life satisfaction: In general, how satisfied are you with your life? Responses ranging from 1 (very satisfied) to 4 (very dissatisfied)

Time frame: 9 weeks after program start

Population: Some participants opted to skip this measure

ArmMeasureValue (MEAN)Dispersion
MentorPROLife Satisfaction2.00 units on a scaleStandard Deviation 0.98
ControlLife Satisfaction1.96 units on a scaleStandard Deviation 0.94
p-value: 0.228Mixed ANOVA
Primary

Self-reported Anxiety Symptoms

General Anxiety Disorder - 7 (GAD-7): Anxiety symptoms over the last two weeks Scores range from 0 (no anxiety symptoms) to 21 (extreme/severe anxiety symptoms)

Time frame: 9 weeks after program start

Population: Some participants opted to skip this measure

ArmMeasureValue (MEAN)Dispersion
MentorPROSelf-reported Anxiety Symptoms6.39 score on a scaleStandard Deviation 5.01
ControlSelf-reported Anxiety Symptoms3.19 score on a scaleStandard Deviation 3.89
p-value: 0.461Mixed ANOVA
Primary

Self-reported Depression Symptoms

Patient Health Questionnaire - 9 (PHQ-9): Depression symptoms over the last two weeks, minus item 9 (suicidal ideation) Scores range from 0 (no depression symptoms) to 24 (high/extreme depression symptoms).

Time frame: 9 weeks after program start

Population: Some participants opted to skip this measure

ArmMeasureValue (MEAN)Dispersion
MentorPROSelf-reported Depression Symptoms8.21 score on a scaleStandard Deviation 4.97
ControlSelf-reported Depression Symptoms3.88 score on a scaleStandard Deviation 3.29
p-value: 0.182Mixed ANOVA
Secondary

Academic Self-efficacy

Single item of feelings of academic self-efficacy: I am confident that I will be a successful student at UMass Boston. Scores range from strongly disagree (1) to strongly agree (5) Greater scores reflect greater perceived academic self-efficacy

Time frame: 9 weeks after program start

Population: Some participants opted to skip this measure

ArmMeasureValue (MEAN)Dispersion
MentorPROAcademic Self-efficacy3.61 units on a scaleStandard Deviation 1.27
ControlAcademic Self-efficacy4.41 units on a scaleStandard Deviation 0.69
p-value: 0.295Mixed ANOVA
Secondary

Cognitive Load

Single item assessing cognitive load of finding resources on campus: It can be exhausting to find the information and resources I need to succeed. Scores range from strongly disagree (1) to strongly agree (5) Greater scores reflect greater perceived exhaustion when finding needed resources

Time frame: 9 weeks after program start

Population: Some participants opted to skip this measure

ArmMeasureValue (MEAN)Dispersion
MentorPROCognitive Load2.87 units on a scaleStandard Deviation 1.22
ControlCognitive Load2.74 units on a scaleStandard Deviation 1.1
p-value: 0.915Mixed ANOVA
Secondary

Sense of Belonging to the University Community

Single item assessing feelings of sense of belonging: I feel part of the UMass Boston community. Scores range from strongly disagree (1) to strongly agree (5) Greater scores reflect greater sense of belonging to the university community

Time frame: 9 weeks after program start

Population: Some participants opted to skip this measure.

ArmMeasureValue (MEAN)Dispersion
MentorPROSense of Belonging to the University Community3.57 units on a scaleStandard Deviation 1.24
ControlSense of Belonging to the University Community4.26 units on a scaleStandard Deviation 0.94
p-value: 0.226Mixed ANOVA

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