- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07399457
A Nature-based Physical Activity Therapy Group for College Students
Development of a Nature-based Physical Activity Toolkit for University Counseling Centers
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
For this study, our research team partnered with two CAPS therapists to develop a new therapy group called Moving Naturally Through Challenges, which focused on nature-based physical activity as a tool for managing symptoms of depression and anxiety. Prior to group implementation, the researchers and therapists collaborated to develop a detailed implementation handbook with weekly lesson plans for the eight group therapy sessions. Next, we conducted a 2-hour training workshop with all CAPS staff to familiarize them with the content and empower them to refer students to the group.
This intervention was delivered as part of group therapy services offered by CAPS. Students seeking services at CAPS whose primary presenting concerns were depression and/or anxiety were encouraged to consider joining the Moving Naturally group. Interested students attended a 30-minute pre-group screening meeting with the group facilitators to ensure it was a good fit for their needs, and then signed a consent form to formalize their enrollment in the study.
The therapy group ran during the spring semester for 8 weeks. Each session lasted 1.5 hours, and included a weekly discussion topic, applied activities for students (e.g., goal setting and planning), and 30 minutes of nature-based physical activity. Activities included walking, hiking, yoga, outdoor games, resistance training, and sport-based activities that were moderate in intensity. Each participant received a Fitbit, yoga mat, resistance band, and water bottle to bring to each session. The group facilitators received training in group fitness instruction prior to leading the group sessions.
To assess changes in mental health outcomes, all students completed the Counseling Center Assessment of Psychological Symptoms upon intake at CAPS, and again upon completion of the therapy group. In addition, students rated their enjoyment of each group therapy session using the Group Session Rating Scale. Participants were asked to wear their Fitbit 24/7 (except when charging) throughout the 8-week duration of the study, and our research team is able to access their data using the Fitabase platform. Additional data and feedback were collected from the therapists who attended the training and facilitated the group.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Kansas
-
Manhattan, Kansas, United States, 66506
- Kansas State University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Attends an intake session at CAPS
- Passes the pre-group screening (therapist and client agree that group is a good fit for student's needs)
Exclusion Criteria:
- Medical condition that prevents safe participation in physical activity (assessed via ACSM risk screener)
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Intervention
Received the Moving Naturally Through Challenges group therapy intervention
|
The intervention included 8 weeks of group therapy.
Each session was 90 minutes and incorporated 30 minutes of nature-based physical activity and 60 minutes of traditional group therapy with content focused on managing anxiety.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Attendance
Time Frame: Weekly across the 8-week intervention
|
The percentage of total group therapy sessions participants attended
|
Weekly across the 8-week intervention
|
|
Group enjoyment and satisfaction
Time Frame: Weekly across the 8-week therapy group
|
Assessed using the Group Session Rating Scale.
Each of the 6 items is rated on a scale from 0-10, with higher scores indicating higher group enjoyment and satisfaction with group relationships, topics, approach, activity, skills, and overall.
|
Weekly across the 8-week therapy group
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Depression and anxiety
Time Frame: Baseline and week 8
|
Measured via the Counseling Center Assessment of Psychological Symptoms (CCAPS).
The depression, general anxiety, and social anxiety subscales are scored on a scale from 0-100, with higher scores indicating greater depression and anxiety.
|
Baseline and week 8
|
Collaborators and Investigators
Sponsor
Collaborators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- IRB-12065
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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