Clinical Trials Logo

Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT03272555
Other study ID # 365
Secondary ID
Status Terminated
Phase N/A
First received August 29, 2017
Last updated April 24, 2018
Start date September 5, 2017
Est. completion date October 13, 2017

Study information

Verified date April 2018
Source Beloit College
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


Description:

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". Results for this study will be quantified through the use of standardized self-report questionnaires administered prior to and after students complete the WILD 5 program. Data will be collected to evaluate participants' adherence and response to each element of WILD 5, a 5-pronged 30-day wellness intervention. It is expected that this 30-day integrated, prescriptive, and trackable program will be found to be an efficacious wellness intervention for First Year Beloit College students.


Recruitment information / eligibility

Status Terminated
Enrollment 14
Est. completion date October 13, 2017
Est. primary completion date October 10, 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- students 18 years of age or older

- students enrolled in First Year Initiative Course titled, "Habits of Mind, Habits of Body."

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 Course titled, "Habits of Mind, Habits of Body".

Study Design


Related Conditions & MeSH terms


Intervention

Other:
WILD 5 Wellness Interventions
Students enrolled in the study will be asked to complete activities in five wellness elements including exercise, mindfulness, sleep, social connectedness and nutrition for 30 days.

Locations

Country Name City State
United States Beloit College Beloit Wisconsin

Sponsors (1)

Lead Sponsor Collaborator
Beloit College

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in Patient Health Questionnaire-9 (PHQ-9) PHQ-9 is a self reported depression scale. Day 0, Day 31+/- 5 days, Day 30+6 months (approximately)
Primary Change in Generalized Anxiety Disorder-7 (GAD-7) GAD-7 is a self-reported questionnaire used to assess anxiety symptoms. Day 0, Day 31+/- 5 days, Day 30+6 months (approximately)
Primary Change in The HERO Wellness Scale The HERO Wellness Scale is a brief scale designed to measure mental wellness specifically happiness, enthusiasm, resilience and optimism. Day 0, Day 31+/- 5 days, Day 30+6 months (approximately)
Primary Change in World Health Organization-5 (WHO-5) WHO-5 is a brief scale that measures mental well-bring. Day 0, Day 31+/- 5 days, Day 30+6 months (approximately)
Primary Change in Cognitive and Physical Functioning Questionnaire (CPFQ) CPFQ is a brief scale that measures cognitive and executive dysfunction. Day 0, Day 31+/- 5 days, Day 30+6 months (approximately)
Secondary The Post-Program Participant Questionnaire The Post-Program Participant Questionnaire is a brief survey that captures participants' opinions about WILD 5 Wellness: A 30-Day Intervention, and subjective ranking of their overall wellness. Day 31+/- 5 days
See also
  Status Clinical Trial Phase
Active, not recruiting NCT05777044 - The Effect of Hatha Yoga on Mental Health N/A
Recruiting NCT04977232 - Adjunctive Game Intervention for Anhedonia in MDD Patients N/A
Recruiting NCT04680611 - Severe Asthma, MepolizumaB and Affect: SAMBA Study
Recruiting NCT04043052 - Mobile Technologies and Post-stroke Depression N/A
Completed NCT04512768 - Treating Comorbid Insomnia in Transdiagnostic Internet-Delivered Cognitive Behaviour Therapy N/A
Recruiting NCT03207828 - Testing Interventions for Patients With Fibromyalgia and Depression N/A
Completed NCT04617015 - Defining and Treating Depression-related Asthma Early Phase 1
Recruiting NCT06011681 - The Rapid Diagnosis of MCI and Depression in Patients Ages 60 and Over
Completed NCT04476446 - An Expanded Access Protocol for Esketamine Treatment in Participants With Treatment Resistant Depression (TRD) Who do Not Have Other Treatment Alternatives Phase 3
Recruiting NCT02783430 - Evaluation of the Initial Prescription of Ketamine and Milnacipran in Depression in Patients With a Progressive Disease Phase 2/Phase 3
Recruiting NCT05563805 - Exploring Virtual Reality Adventure Training Exergaming N/A
Completed NCT04598165 - Mobile WACh NEO: Mobile Solutions for Neonatal Health and Maternal Support N/A
Completed NCT03457714 - Guided Internet Delivered Cognitive-Behaviour Therapy for Persons With Spinal Cord Injury: A Feasibility Trial
Recruiting NCT05956912 - Implementing Group Metacognitive Therapy in Cardiac Rehabilitation Services (PATHWAY-Beacons)
Completed NCT05588622 - Meru Health Program for Cancer Patients With Depression and Anxiety N/A
Recruiting NCT05234476 - Behavioral Activation Plus Savoring for University Students N/A
Active, not recruiting NCT05006976 - A Naturalistic Trial of Nudging Clinicians in the Norwegian Sickness Absence Clinic. The NSAC Nudge Study N/A
Enrolling by invitation NCT03276585 - Night in Japan Home Sleep Monitoring Study
Completed NCT03167372 - Pilot Comparison of N-of-1 Trials of Light Therapy N/A
Terminated NCT03275571 - HIV, Computerized Depression Therapy & Cognition N/A