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CompletedNCT06003920Updated Aug 22, 2023

Outcomes of a Small Process Group on Medical Students' Grit, Resilience, and Stress

An interventional study of Process group in Stress, sponsored by Western University of Health Sciences. Completed at 1 site in United States. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2023-08-22.

Sponsored by Western University of Health Sciences · Not applicable, Interventional, and Supportive care

From the registry’s dates

  • Registered 1 year 1 month after the study started (first participant enrolled Jun 2022, registered Jul 2023).
Phase
Not applicable
Study type
Interventional
Enrollment
16
Allocation
Non-randomized
Ages
18 Years and older
Sex
All
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Study summary

The incidence of burnout and mental ill-health begins very early in medical school and continues to be high throughout training. Medical students are under high amounts of stress, which often becomes chronic, and can lead to both physical and psychological issues as a student, resident, and physician. Chronic stress and burnout in medical students are not a new phenomenon, but recent research has highlighted the worsening mental health of medical students, with as high as three-quarters of students reporting mental ill-health. It is vital that ways are found to reduce burnout and assist in improving the mental health of medical students. This quasi-experimental study aimed to assess the effect of a small process group vs. a control group of preclinical medical students on their stress, resilience, and grit.

Read the detailed description

The investigators assessed the effects of a year-long small process group intervention, led by a psychiatrist, which aimed to improve self-awareness, mindfulness, and resilience in first and second-year medical students. Students self-selected into the process group, and the same number were randomly recruited as controls from the rest of the preclinical student body. The psychiatrist who led the groups was blinded to student participation in the study. Students in the process and control groups were surveyed with the Perceived Stress Scale, the Connor-Davidson Resilience Scale, and the Grit Scale in September 2022, and again after nine months and 25 sessions, in May 2023, after the academic year. Statistical analysis was done with R Studio. Bandura's theory of self-efficacy was used to conceptualize the study. Recruitment was done by email, as was data collection. The intervention included guided exploration of the psychodynamic process, group dynamic theory, cognitive behavioral therapy, dialectical behavioral therapy, boundaries, and empathy.

02

Conditions studied

  • Stress

Keywords

  • medical students
  • stress
  • grit
  • resilience
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In context

Lead sponsor

Western University of Health Sciences is the lead sponsor of 21 studies on the registry; 2 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  1. The participant must be an enrolled student at the College of Osteopathic Medicine of the Pacific-NW
  2. Participant must be in their first or second year of medical school
  3. Participant must be at least 18 years of age
  4. Participant must self-select into either the intervention group or control group
  5. Participant must sign informed consent

Exclusion criteria

Exclusion Criteria:

  1. Data will be excluded if a student goes on a LOA during the course of the year
  2. Data will be excluded if a student does not attend a minimum of 12 out of 25 small group sessions
  3. Student does not give informed consent
  4. Student withdraws consent at any time
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Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
Single (Care provider)
Enrollment
16 participants (actual)

Study arms

  • Experimental
    Process Group

    Medical students enrolled in the small process group, led by psychiatrist.

    Behavioral: Process group

  • No intervention
    Control Group

    Medical students from the same cohorts, not enrolled in the small process group.

Interventions

  • BehavioralProcess group

    The medical student process group served as a space for students to gain increased self-awareness through guided exploration of the psychodynamic processes.

06

What researchers measure

Primary outcomes

  1. Perceived Stress Scale-14

    Stress measured on a 0-56 scale; higher number means more stress. Each of the 14 questions is measured on a 0-4 scale of 0 = Never, 1 = Almost Never, 2 = Sometimes, 3 = Fairly Often, 4 = Very Often.

    Time frame: 34 weeks

  2. Connor-Davidson Resilience Scale-25

    Resilience is measured on this 25-item scale, with higher numbers meaning more resilience. The score can range between 0 and 100. Each item has anchors from 0-4.

    Time frame: 34 weeks

  3. The Grit Scale

    The original 12-item grit scale was used to measure grit; each items is rated 1-5, then scores are summed and divided by 12, so the final score is between 1-5. Higher scores mean more grit.

    Time frame: 34 weeks

Secondary outcomes

  1. Medication or diagnosis change

    Change in anti-depression, anti-anxiety, or other mental health medications or diagnoses on a binary yes/no scale.

    Time frame: 34 weeks

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Study locations

1 site
  • College of Osteopathic Medicine of the Pacific - Northwest
    Lebanon, Oregon 97355, United States
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References and documents

Study documents

  • Informed consent form · Jun 24, 2022

Documents are hosted by the registry — open the source record to download them.

Individual participant data

Plan to share: Yes — All anonymized demographic and outcome data will be shared in an open-access data repository.

Supporting information: Study protocol, Sap, Icf

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 22, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT06003920
Lead sponsor
Western University of Health Sciences
Responsible party
Edie Sperling (Assistant Professor and Vice-Chair, Medical Anatomical Sciences, Western University of Health Sciences) — Principal investigator
First posted
Aug 22, 2023
Start date
Jun 24, 2022
Primary completion
May 30, 2023
Completion
May 30, 2023
Last update
Aug 22, 2023

Study contacts

Edie L Sperling, DPT
principal investigator · Western University of Health Sciences

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Aug 2023. You cannot join it, but the record below documents what was studied.

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