A Nature-based Physical Activity Therapy Group for College Students

February 2, 2026 updated by: Emily Mailey, Kansas State University

Development of a Nature-based Physical Activity Toolkit for University Counseling Centers

This study examined the feasibility, acceptability, and preliminary effectiveness of a nature-based physical activity group delivered by K-State Counseling and Psychological Services (CAPS) for students experiencing depression and anxiety.

Study Overview

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

Interventional

Enrollment (Actual)

6

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Kansas
      • Manhattan, Kansas, United States, 66506
        • Kansas State University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

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

This section provides details of the study plan, including how the study is designed and what the study is measuring.

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:
  • nature-based physical activity therapy group

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

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

February 1, 2025

Primary Completion (Actual)

June 30, 2025

Study Completion (Actual)

June 30, 2025

Study Registration Dates

First Submitted

January 26, 2026

First Submitted That Met QC Criteria

February 2, 2026

First Posted (Actual)

February 10, 2026

Study Record Updates

Last Update Posted (Actual)

February 10, 2026

Last Update Submitted That Met QC Criteria

February 2, 2026

Last Verified

February 1, 2026

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

IPD Plan Description

Data is private health information.

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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