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Addressing Sleep Problems in Older Adults

To Sleep, Perchance to Dream: A Randomized, Placebo-Controlled Study to Test a Fruit/Honey-Based Foodstuff for Sleep Problems in Older Adults

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02593981
Enrollment
0
Registered
2015-11-02
Start date
2018-03-31
Completion date
2019-04-30
Last updated
2018-12-11

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

Conditions

Sleep

Keywords

sleep, fruit, honey, geriatric

Brief summary

As many as 57% of older adults complain of major disruption of sleep, 29% struggle to fall asleep and 19% complain of early-morning awakening. The implications of this sleep deprivation are sobering, particularly among older individuals. The primary goal of this study is to determine whether a palatable foodstuff which contains a fruit/honey drink and which is taken every evening before bedtime leads to improved sleep in community-living individuals with sleep problems.

Detailed description

This is a randomized, placebo-controlled double-blinded pilot study to explore the use of a fruit/honey drink product for improving sleep in older adults. The purpose of this study is to estimate the effects of a fruit/honey drink using various assessment tools when used as short-term intervention. This trial proposes to enroll a total of 60 community based older adults. All study patients will be instructed to take the study product every day for 28 days. During which time, study subjects will return weekly to complete study visits for a total of 4 visits.

Interventions

DIETARY_SUPPLEMENTFruit/Honey drink

2 canisters of powder containing fruit/honey mix to be mixed with water and ingested twice a day for 28 days

DIETARY_SUPPLEMENTPlacebo

2 canisters of Placebo powder containing non-active ingredient to be mixed with water and ingested twice a day for 28 days

Sponsors

Mayo Clinic
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
60 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

1. Age ≥ 60 years old at the time of study registration. 2. Individual describes trouble either falling asleep or staying asleep at study entry. 3. Willing to participate in all aspects of the study. 4. Willing to avoid kiwifruit, cherry, and honey for 4 weeks while on this study. 5. Willing to avoid changes to current sleep medications (may use a stable dose of a currently prescribe sleep medication during the first 4 weeks after stating the intervention).

Exclusion criteria

1. Allergic to kiwifruit, cherries, honey, apples, or bananas. 2. Hospitalized or living in a care facility at the time of enrollment. 3. Clinical evidence of active malignant disease (cancer), as per healthcare provider's clinical judgment. 4. Any cancer therapy (for example, chemotherapy, hormonal therapy, radiation, surgery, immunotherapy) in the preceding 3 months. 5. Healthcare provider does not think that study candidate has a specific health problem that precludes participation. 6. Allergy or intolerance of milk products. 7. Women of child bearing potential.

Design outcomes

Primary

MeasureTime frameDescription
PSQI score28 daysPittsburgh Sleep Quality Index (PSQI):

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026