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Mind Body Interventions for the Student Population

Mind Body Interventions for the Student Population

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03756701
Enrollment
20
Registered
2018-11-28
Start date
2018-09-15
Completion date
2019-05-01
Last updated
2021-04-28

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

Conditions

Anxiety, Chronic Pain, Stress

Brief summary

This crossover randomized design study's objective is to see if mind body interventions can help students on a college campus manage their chronic pain and/or PTSD. Participants will attend 10 mind body skills group sessions that are 2 hours each. These group sessions teach a variety of ways (skills) for people to express their feelings. A licensed doctor, who is certified to teach mind-body skills group classes, will lead the skills group. Participants will be assessed with an anxiety questionnaire, a chronic pain measure and a measure of heart rate variability. There will be two groups. Group 1 will begin intervention after baseline testing and will receive follow-up skill sessions once every month for 6 months. The first group will also attend bonus classes during the next 6 months. The second group will do baseline testing and no intervention for the first 10 weeks. They will then participate in the skills groups the second 10 weeks. There will be 3,6 and 12 month follow up data also taken.

Detailed description

Students on campus will be made aware of the study through fliers posted on campus. If they contact the study representatives to participate, they will fill out a screening questionnaire that will determine their symptoms and care they are currently receiving. Those that meet the inclusion criteria will be assigned to Group 1 or 2 randomly. The mind body skills groups will be 10 weeks long. Group 1 will participate in mind body interventions immediately, and Group 2 will continue with their usual care for the 10 weeks. After the first session, Group 2 will complete the mind body intervention sessions. The research will therefore be a crossover randomized design where each group will serve as its own control, and also may be compared to the other group. Participants in either group will still be allowed to participate in any care they are currently receiving outside of the mind body intervention, including but not limited to counseling or a support group or therapy. Also, after these groups are over, the first group will continue to have reunion groups once per month for 6 months and the second group will not. Reunion groups will consist of supplementary mind body skills group sessions that reinforce skills learned in the original mind body skills groups and also work on retention of knowledge beyond the program. Outcome measures will be taken pre and post mind body skills group, and then at 3, 6, and 12 months after the 10 week mind body skills group ends. The topics for each session is based upon the Centers for Mind Body Medicine model. Both groups will follow this same weekly topic schedule. 1. Introduction and Drawings 2. Autogenic Training and Biofeedback 3. Guided Imagery 4. Meditation 5. Mobilizing, Transforming, and Celebrating Emotion 6. Genograms part 1 7. Genograms part 2 8. Mindful Eating and Healthy Nutrition 9. Spirituality 10. Closing Drawings and Ritual

Interventions

BEHAVIORALMind body skills

2 hour skill sessions that focus on mindfulness: The topics for each session is based upon the Centers for Mind Body Medicine model. Both groups will follow this same weekly topic schedule. 1. Introduction and Drawings 2. Autogenic Training and Biofeedback 3. Guided Imagery 4. Meditation 5. Mobilizing, Transforming, and Celebrating Emotion 6. Genograms part 1 7. Genograms part 2 8. Mindful Eating and Healthy Nutrition 9. Spirituality 10. Closing Drawings and Ritual

Sponsors

Youngstown State University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

There will be 2 groups of participants. Group 1 will begin the intervention immediately. Group 2 will maintain their usual lifestyle for the first 10 weeks, and begin group sessions when group 1 has completed. There will be refresher sessions for group 1 once per month, and 3, 6 12 month follow up testing after the group sessions.

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

Selection criteria includes: Students aged 18-65 who own a smartphone that is able to download the HRV4Training app. Students must be enrolled in graduate or undergraduate classes on Youngstown State University's campus.

Exclusion criteria

students that have had previous experience with mind body skills groups or stress reduction interventions within the past 12 months. \-

Design outcomes

Primary

MeasureTime frameDescription
Change in Post Traumatic Stress Disorder Checklist - Civilian (PCLC)Pre intervention, post intervention, 3,6,12 month followupQuestionnaire
Change in Graded Chronic Pain ScalePre intervention, post intervention, 3,6,12 month followupQuestionnaire
Change in Patient Health Questionnaire - 9 (PHQ 9),Pre intervention, post intervention, 3,6,12 month followupQuestionnaire
Change in Five Facet Mindfulness Questionnaire - 15 (FFMQ - 15)Pre intervention, post intervention, 3,6,12 month followupQuestionnaire
Change in Heart rate variabilityPre intervention, post intervention, at the start of each session, 3,6,12 month followupMeasure of heart rate change over time taken with an ap on a cell phone.

Countries

United States

Outcome results

None listed

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