Effect of Sleep Deprivation on Sensory Integration of Balance, Fall Risk and Postural Stability

NCT ID: NCT05170191

Last Updated: 2021-12-27

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

UNKNOWN

Total Enrollment

30 participants

Study Classification

OBSERVATIONAL

Study Start Date

2021-12-30

Study Completion Date

2022-05-30

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

Sleepiness caused by sleep deprivation may increase the risk of injuries and damages during physical activity. Individual data so far indicates worsening of postural stability and control with females exhibiting better static postural stability regardless of sleeping conditions in comparison to men. However, the literature is deficient in terms of postural stability conditions with eyes open and eyes closed states, as well as fall risk and sensory integration of balance.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Sleep Deprivation

Keywords

Explore important study keywords that can help with search, categorization, and topic discovery.

sleep deprivation

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Sleep deprivation

Participant data will be acquired before and after 24 hours of sleep deprivation.

Sleep Deprivation

Intervention Type BEHAVIORAL

The participants will stay awake for 24 hours.

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Sleep Deprivation

The participants will stay awake for 24 hours.

Intervention Type BEHAVIORAL

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Age 19 to 24
* Healthy young adults from Rawalpindi/Islamabad.
* Both males and females
* Participants should have normal sleep patterns without any signs or symptoms of insomnia or hypersomnia.
* Persons without any sleep disorders.
* Persons without any neurological disease.

Exclusion Criteria

* Persons with sleep disorders such as hypersomnia, insomnia, parasomnia etc.
* Elderly population.
* Persons with any sort of neurological deficits.
* COVID positive and those with any suspected signs and symptoms of COVID-19.
* Alcoholics
* Pregnant females
* A participant with the history of or active diagnosed conditions of any of the following, which renders individual's performance will be excluded:

* Neurological.
* Musculoskeletal.
* Cardiopulmonary.
* Any congenital disorder or limb deformities.
Minimum Eligible Age

19 Years

Maximum Eligible Age

24 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Foundation University Islamabad

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Foundation University Institute of Rehabilitation Sciences.

Islamabad, Federal, Pakistan

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Pakistan

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

FUI/CTR/2021/8

Identifier Type: -

Identifier Source: org_study_id