ClinicalTrials.gg
CompletedNCT03328520Updated Apr 26, 2018

WILD 5 Wellness, A 30-Day Intervention

An interventional study of WILD 5 Wellness Intervention in Anxiety, Depression and Cognitive Functioning, sponsored by Beloit College. Completed at 1 site in United States. Open to participants aged 17 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2018-04-26.

Primary conditionDepressionRegistry: Anxiety DisordersReclassifiedWhy we changed it
Registry
Anxiety Disorders — the first condition term the registry derived for this study.
ClinicalTrials.gg
Depression
Why
  1. The registry often attaches Anxiety Disorders to studies about something else, and this study's title and listed conditions do not name it.
  2. The study's listed conditions name Depression.
Confidence
High: the new condition is named in the study's own listed conditions. Of 351 hand-checked studies reclassified this way, 68% were exactly right and 84% in the right disease family; the registry's first term was right for 5% (measured 2026-10-21). How we classify →
Wrong?
Tell us the study's main condition →

Sponsored by Beloit College · Not applicable, Interventional, and Other

Help build ClinicalTrials.gg — short surveys, remote interviews or testing, in your language. Take part →

Phase
Not applicable
Study type
Interventional
Enrollment
33
Allocation
Not applicable
Ages
17 Years and older
Sex
All
01

Where this study stands

Counted across the records on this site · 2026-11-13

Among 3,709 studies in Depression with a site in United States — 578 open to participants now, 717 under way, 30 of them phase 3. Depression · United States.

Enrollment
2,387th of 3,316
33 · median 72
Started
2017
with 140 others
No phase
2,215 of 3,709
384 open now
Registered
1,917th of 3,709
by date

Among the 3,709 studies in Depression with a site in United States, this one is the 2,387th largest by enrollment of the 3,316 interventional ones that give a count, is one of 141 that started in 2017, is one of 2,215 with no phase, and was the 1,917th registered.

Depression

8,582 studies on the registry are indexed under Depression; 1,723 are open to participants now.

Browse Depression studies →

Open to participants now

578 of the 3,709 studies in Depression with a site in United States are open now. Recruiting first, the newest first:

573 more — sign in →

All 578 open studies →

A study can be open while its sites in United States have not opened yet or have stopped. Only those recruiting at a site in United States →

Who these studies take

Of the 1,089 Depression studies recruiting now, 470 (43%) set no upper age limit and 519 (48%) stop at 75 or younger; 203 take children under 18; 311 take healthy volunteers.

This study: 17 Years and older · all sexes · healthy volunteers too.

The full table on the hub →

This tab as a report to print or save as PDF → With an account.

Was this useful?
Watch this landscapeDownload CSVNarrow it in search →With an account: a weekly mail of what changed among 3,709 studies in Depression with a site in United States, or all of them as a file.
02

Study summary

The purpose of this study is to explore the efficacy and feasibility of an integrated, prescriptive, and trackable wellness intervention combining five wellness elements including exercise, mindfulness, sleep, social connectedness, and nutrition in First Year Beloit College students self-selected into a wellness focused first year initiative. This program is called "WILD 5 Wellness: A 30-Day Intervention".

03

Conditions studied

  • Anxiety
  • Depression
  • Cognitive Functioning
  • Wellness

Browse trials for

04

In context

Depression Reclassified

8,582 studies on the registry are indexed under Depression; 1,723 are open to participants now.

This study's enrollment of 33 is below the median of 81 across 7,066 interventional studies indexed under Depression.

Browse Depression studies →

Lead sponsor

Beloit College is the lead sponsor of 3 studies on the registry; none are open to participants now.

Compared within Depression, this study's primary condition as ClinicalTrials.gg classifies it; the registry's first condition term is Anxiety Disorders. The counts are of registry records indexed under each term, refreshed daily. How we classify →

05

Who can participate

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

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

  • Students 18 years of age or older or 17 years of age with legal guardian written permission.
  • Students enrolled in First Year Initiative Courses titled "Balance" or "Constructing Health"

Exclusion criteria

Exclusion Criteria:

  • Individuals who are pregnant or plan to get pregnant during the next 30 days.
  • Students who are not enrolled in the First Year Initiative Courses titled "Balance" or "Constructing Health"
06

Study design

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

Study arms

  • Experimental
    First Year Students in Wellness FYIs

    Behavioral: WILD 5 Wellness Intervention

Interventions

  • BehavioralWILD 5 Wellness Intervention

    Behaviors in 6 areas of wellness: Sleep, Social Connectedness, Exercise, Nutrition, Mindfulness and "HERO" (Happiness, Enthusiasm, Resilience, Optimism)

07

What researchers measure

Primary outcomes

  1. Change in Patient Health Questionnaire-9 (PHQ-9)

    PHQ-9 is a self reported depression scale. It is a 9-item scale with scores ranging from 0-27. Lower scores denote improvement.

    Time frame: Day 0, Day 30+ 3 days (approximately)

  2. Change in Generalized Anxiety Disorder-7 (GAD-7)

    GAD-7 is a self-reported questionnaire used to assess anxiety symptoms. It is a 7-item scale with scores ranging from 0-21. Lower score denotes improvement.

    Time frame: Day 0, Day 30+ 3 days (approximately)

  3. Change in the HERO Wellness Scale

    HERO Wellness Scale is a brief scale designed to measure mental wellness specifically happiness, enthusiasm, resilience and optimism. It is a 5-item scale with scores ranging from 0-10. Higher score denotes improvement.

    Time frame: Day 0, Day 30+ 3 days (approximately)

  4. Change in World Health Organization-5 (WHO-5)

    WHO-5 is a brief scale that measures mental well-being. It is a 5-item scale with scores ranging from 0-25. Higher score denotes improvement.

    Time frame: Day 0, Day 30+ 3 days (approximately)

  5. Change in Cognitive and Physical Functioning Questionnaire (CPFQ)

    CPFQ is a brief scale that measures cognitive and executive dysfunction. It is a 7-item scale with scores ranging from 7-42. Lower score denotes improvement.

    Time frame: Day 0, Day 30+ 3 days (approximately)

Secondary outcomes

  1. The Post-Program Participant Questionnaire

    The Post-Program Participant Questionnaire is a brief survey that captures participants'opinions about WILD 5 Wellness.

    Time frame: Day 30+ 3 days (approximately)

08

Study locations

1 site
  • Beloit College
    Beloit, Wisconsin 53511, United States
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 Oct 2017 to primary completion in Nov 2017, 1 month.

Of 3,471 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 1 month is below that.

Counting every sponsor, half of 3,569 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
Oct 20, 2017
First posted
Nov 1, 2017
StartActual
Oct 24, 2017
Primary completionActual
Nov 29, 2017
CompletionActual
Nov 29, 2017
Last update
Apr 26, 2018
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 Apr 26, 2018, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03328520
Lead sponsor
Beloit College
Responsible party
Sponsor
First posted
Nov 1, 2017
Start date
Oct 24, 2017
Primary completion
Nov 29, 2017
Completion
Nov 29, 2017
Last update
Apr 26, 2018

Study contacts

Tara M Girard, BSN
principal investigator · Beloit College
Suzanne Cox, PhD
principal investigator · Beloit College
Laura Parmentier, PhD
principal investigator · Beloit College
Saundra Jain, PsyD, LPC
principal investigator · Beloit College
Rakesh Jain, MD, MPH
principal investigator · Beloit College

Oversight

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 Apr 2018. 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