ClinicalTrials.gg
CompletedNCT07399457Updated Feb 10, 2026

A Nature-based Physical Activity Therapy Group for College Students

An interventional study of Moving Naturally Through Challenges group therapy in Depression and Anxiety Symptom, sponsored by Kansas State University. Completed at 1 site in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-02-10.

Sponsored by Kansas State University · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 11 months after the study started (first participant enrolled Feb 2025, registered Jan 2026).
Phase
Not applicable
Study type
Interventional
Enrollment
6
Allocation
Not applicable
Ages
18 Years and older
Sex
All
01

Study summary

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.

Read the 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.

02

Conditions studied

  • Depression and Anxiety Symptom

Keywords

  • anxiety
  • college students
  • physical activity
  • nature
  • group therapy
03

In context

Depression

8,577 studies on the registry are indexed under Depression; 1,720 are open to participants now.

This study's enrollment of 6 is below the median of 81 across 7,063 interventional studies indexed under Depression.

Browse Depression studies →

Lead sponsor

Kansas State University is the lead sponsor of 31 studies on the registry; 5 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

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

Exclusion Criteria:

  • Medical condition that prevents safe participation in physical activity (assessed via ACSM risk screener)
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
6 participants (actual)

Study arms

  • Experimental
    Intervention

    Received the Moving Naturally Through Challenges group therapy intervention

    Behavioral: Moving Naturally Through Challenges group therapy

Interventions

  • BehavioralMoving Naturally Through Challenges group therapy

    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.

    Also known as: nature-based physical activity therapy group

06

What researchers measure

Primary outcomes

  1. Attendance

    The percentage of total group therapy sessions participants attended

    Time frame: Weekly across the 8-week intervention

  2. Group enjoyment and satisfaction

    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.

    Time frame: Weekly across the 8-week therapy group

Secondary outcomes

  1. Depression and anxiety

    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.

    Time frame: Baseline and week 8

07

Study locations

1 site
  • Kansas State University
    Manhattan, Kansas 66506, United States
08

References and documents

Individual participant data

Plan to share: Undecided — Data is private health information.

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Ran from Feb 2025 to primary completion in Jun 2025, 4 months.

Of 3,468 non-industry interventional studies with no phase under Depression, half reached primary completion within 21 months of starting (the median), counting those still running; a quarter within 10 and three quarters within 41. This study's 4 months is below that.

Counting every sponsor, half of 3,566 studies reached it within 21 months; a quarter within 9 and three quarters within 41.

How these figures are worked out, and which studies are left out of them.

Registered
Jan 26, 2026
First posted
Feb 10, 2026
StartActual
Feb 1, 2025
Primary completionActual
Jun 30, 2025
CompletionActual
Jun 30, 2025
Last update
Feb 10, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Feb 10, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07399457
Lead sponsor
Kansas State University
Collaborators
Frontiers Clinical & Translational Science Institute
Responsible party
Emily Mailey (Associate Professor, Kansas State University) — Principal investigator
First posted
Feb 10, 2026
Start date
Feb 1, 2025
Primary completion
Jun 30, 2025
Completion
Jun 30, 2025
Last update
Feb 10, 2026

Oversight

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

Not currently enrolling

This study is completed, as verified in Feb 2026. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion