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Prescribing Laughter for Sleep and Wellbeing in UAE University Students

Can a Laughter Prescription Improve Psychological Health, Wellbeing, and Sleep in Zayed University Students?

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04171245
Enrollment
40
Registered
2019-11-20
Start date
2019-09-26
Completion date
2020-04-15
Last updated
2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Mental Health Wellness, Sleep

Keywords

Sleep, laughter, well-being, mental health

Brief summary

This study is in line with the UAEs national drive to promote happiness and wellbeing. University students risk impaired psychological health, wellbeing, and sleep due to academic pressures. This research is the first to assess the feasibility of using a laughter prescription to improve psychological health and sleep in Zayed University students. Forty students will be recruited, and randomized to a control or laughter group.

Detailed description

The Laughie is a self created app or tool. It is a one minute recording of the user's joyful laughter on their smartphone. Once recorded, the user uses it by playing back the recording and laughing with it for the duration of the one minute. The Laughie acts as a prompt to guide the one minute of laughter. In this research the experimental group each record their own Laughie, demonstrated and supported by the PI(s). They are then prescribed to laugh with their Laughie: 3x a day the first week (morning, lunch, and afternoon) and at least 2x a day during the second week. Immediately after using their Laughie they fill in a Laughie checklist to record whether they laughed for the full minute, whether they enjoyed their Laughie, and how they felt afterwards. This study tracks sleep using wrist actigraphy in the control group (no Laughie prescription) and in the Laughie group. All participants complete one week baseline using sleep watches, and sleep diaries, prior to the Laughie intervention. They all then continue to track their sleep during the intervention. All participants complete WHO Five well-being, PSKI, and HADS pre and post intervention. During the intervention the Laughie participants complete Laughie checklists. All participants are invited for a final interview (the control group about the sleep equipment experience). A follow-up survey is sent to the Laughie group 2 months after their prescription.

Interventions

OTHERLaughie laughter prescription

Creation of a Laughie; laughing with their Laughie 3x a day

DEVICESleep tracking equipment

Tracking sleep using equipment

Sponsors

Zayed University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 50 Years
Healthy volunteers
Yes

Inclusion criteria

Registered Zayed University students, owner of a smartphone -

Exclusion criteria

Chronic health conditions (cardiovascular disease, respiratory disease, cancer, diabetes), deafness, non-English speakers \-

Design outcomes

Primary

MeasureTime frameDescription
Feasibility of two-week laughter prescription6 monthsUsing the Laughie. Evaluate with Laughie checklists and interviews

Secondary

MeasureTime frameDescription
Assess if overall well-being improves6 monthsUsing WHO Five, Laughie checklists, and interviews
Assess if specific aspects of wellbeing improve6 monthsUsing WHO Five, Laughie checklists, interviews
Assess if mental health improves6 monthsUsing HADS, interviews
Assess if subjective sleep outcomes improve6 monthsUsing PSKI and interviews
Assess if objective sleep outcomes improve6 monthsUsing wrist actigraphy

Countries

United Arab Emirates

Contacts

Primary ContactTeresa Arora, PhD
Teresa.Arora@zu.ac.ae+971 2 599 3160

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 25, 2026