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Trial · NCT07880054

Sleep Quality and Frailty Among People Living With HIV

NCT07880054, Completed, National Sun Yat-sen University

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Sleep Quality and Frailty Among People Living With HIV. Trials, record NCT07880054. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07880054

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Sleep Quality and Frailty Among People Living With HIV
NCT number
NCT07880054
Status
Completed
Enrollment
130 participants, actual
Lead sponsor
National Sun Yat-sen University
Conditions
HIV Infections, Frailty, Sleep Quality, Oral Frailty
Interventions
No intervention (observational assessments)
First posted
2026-10-19
Last updated
2026-10-19

Source ClinicalTrials.gov

Registered outcomes13

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryPrevalence of oral hypofunctionBaseline (single study visit)
Oral function evaluated using the seven-domain framework of the Japanese Society of Gerodontology: oral hygiene, masticatory function, swallowing function, occlusal force, oral dryness, tongue-lip motor function (oral diadochokinesis), and tongue pressure. Oral hypofunction is defined as impairment in at least three of the seven domains. Reported as the proportion of participants with oral hypofunction in each group.
PrimaryNumber of impaired oral function domainsBaseline (single study visit)
Count of impaired domains (range 0-7) within the seven-domain oral hypofunction framework (oral hygiene, masticatory function, swallowing function, occlusal force, oral dryness, tongue-lip motor function, tongue pressure). Higher scores indicate greater oral functional impairment.
PrimaryPhysical frailty score (Fried frailty phenotype)Baseline (single study visit)
Fried frailty phenotype comprising five criteria: unintentional weight loss, self-reported exhaustion, muscle weakness (grip strength), slowness (gait speed), and low physical activity (International Physical Activity Questionnaire). Continuous score range 0-5; robust = 0, pre-frail = 1-2, frail = 3-5. Higher scores indicate greater frailty.
SecondaryInsomnia severity (Insomnia Severity Index, ISI)Baseline7-item self-report questionnaire; total score range 0-28, higher scores indicate more severe insomnia. Clinically relevant insomnia defined as ISI \>= 8.
SecondaryDaytime sleepiness (Epworth Sleepiness Scale, ESS)Baseline8-item self-report scale (Chinese version); total score range 0-24, higher scores indicate greater daytime sleepiness. Excessive daytime sleepiness defined as ESS \> 10.
SecondaryDomain-specific oral hypofunction componentsBaseline
Proportion of participants with impairment in each of the seven oral function domains (oral hygiene, masticatory function, swallowing function, occlusal force, oral dryness, tongue-lip motor function, tongue pressure).
SecondaryNutritional status (Mini Nutritional Assessment-Short Form, MNA-SF)BaselineMNA-SF total score range 0-14; lower scores indicate poorer nutritional status (0-7 malnourished, 8-11 at risk of malnutrition, 12-14 normal).
SecondaryPhysical activity (International Physical Activity Questionnaire, IPAQ)BaselineSelf-reported physical activity expressed as MET-minutes per week; used to define the low physical activity criterion of the Fried frailty phenotype.
SecondaryAnxiety and depression (Hospital Anxiety and Depression Scale, HADS)Baseline14-item scale with anxiety and depression subscales (each 0-21); higher scores indicate more severe symptoms.
SecondaryCognitive function (Mini-Mental State Examination, MMSE)BaselineMMSE total score range 0-30; higher scores indicate better cognitive function; a score \<= 23 suggests cognitive impairment.

Outcomes0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

None in this release.

Results by group0

Each measurement the trial posted, group by group, in the words and numbers it posted.

None in this release.

Participant flow0

How many started, completed or left each group, period by period.

None in this release.

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals0

The totals the trial posted for each group.

None in this release.

Papers0

The papers the trial lists on ClinicalTrials.gov.

None in this release.

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

None in this release.

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT07880054

GET https://conductscience.org/api/trials/v1/NCT07880054/registered