Sleep, Inadequate

2

Review clinical trials related to Sleep, Inadequate. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Impact of Sleep Duration on Immune Balance in Urban Children With Asthma

Urban children with asthma are at high risk for short sleep, due to an environment that jeopardizes both sleep and asthma management. Further, urban children with asthma suffer from altered immune balance, a key biological process contributing to individual differences in asthma morbidity and sleep health. In the proposed research, the researchers will examine the effects of shortened and recovery sleep on immune balance and associated changes in lung function in urban children with allergic asthma through an experimental design.

Participants needed: 204
Trial details
Age: 7-11Biological sex: AllType: InterventionalSponsor: Rhode Island HospitalUpdated: Sep 22, 2025Locations: 1
Eligibility criteria

Children 7-11 years old [+16]

Status: Not yet recruiting

The Effects of Repeated Operational Stress and Limited Recovery on Resilience Capacity

This longitudinal study will examine the effects of repeated bouts of operational stress and limited recovery on integrated MPS, whole-body protein balance, iron absorption, and aerobic performance. Following baseline characterization measures, active adults (n=24) representative of normal weight phenotype (NW; n=12) and overweight phenotype (OW; n=12) will complete a 48h balance phase preceding two rounds of repeated 72h energy deficit exposure each immediately followed by a 48h recovery phase. NW cutoff will be defined ≤ 22% body fat for males and ≤ 32% body fat for females. OW cutoff will be defined as \>22% body fat for males and \>32% body fat for females. These body composition cutoffs are informed by the maximum allowable percent body fat standards outlined in current Army Regulation 600-9. Additional details for determining % body fat are outlined in the experimental procedures section of the protocol.

Participants needed: 24
Trial details
Age: 17-39Biological sex: AllType: InterventionalSponsor: United States Army Research Institute of Environmental MedicineUpdated: Jan 20, 2025Locations: 1
Eligibility criteria

Men and women aged 18 - 39 years (17 - 39 years if military personnel) [+6]

Musculoskeletal injuries that compromise exercise capability as determined by OM... [+10]