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The effect of Zinc Supplementation on Sleep quality and fatigue in the elderly

The effect of Zinc Supplementation on Sleep quality and fatigue in the elderly

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017080635110N2
Enrollment
150
Registered
2017-09-07
Start date
2017-09-23
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Condition 1: Sleep Quality. Condition 2: Fatigue. Sleep disorders Malaise and fatigue

Interventions

Intervention 1: In the intervention group: Zinc supplemented pill is a zinc gluconate form and it contains 30 mg zinc for 70 days will be given to elderly group intervention. One day one of these pill
Treatment - Drugs

Sponsors

Vice chancellor for research - Shahroud University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 100 Years

Inclusion criteria

Inclusion criteria: "The inclusion criteria for this study are": having full satisfaction to participate in this study; seniors 60 years and older; Iranian citizenship; the ability to speak Farsi and answer questions; not using Zinc Supplement; no cognitive impairment (for the elderly with literacy based on the MMSE questionnaire score 25 and more and for the illiterate elderly, based on the AMTS questionnaire, score 7 and more); lack of liver and intestinal diseases to diagnose a doctor, people with serum zinc levels in them based on experiment within be normal range; in that sense people whose serum zinc level is higher or lower than normal range do not enter the study. Elderly people with low sleep quality; according to Pittsburgh sleep quality questionnaire, gaining a score of over 5 in the entire questionnaire is means poor sleep quality. "The exclusion criteria for this study are": the lack of cooperation and refusal of the elderly to continue to participate in research; the consumption of zinc supplement in the control group during the course of 70 days of intervention; the occurrence of severe stress, such as hospitalization or death of relatives in both groups during the study; those who did not use sleep medications before the intervention began but after the intervention begins and in the 70-day study period taking a sleep medication will be excluded.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Sleep Quality. Timepoint: Before the intervention and 70 days after the intervention began. Method of measurement: PSQI standard questionnaire.;Fatigue. Timepoint: Before the intervention and 70 days after the intervention began. Method of measurement: MFI standard questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAbolfazl Afzali

Shahroud University of Medical Sciences

Afzali.a1373@shmu.ac.ir+98 23 3239 5054

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026