Trial on the Effect of Optically Modified Fiber Mattress Covers on Sleep Disturbances in Patients With Chronic Back Pain

University of California Irvine (UCI) logo

University of California Irvine (UCI)

Status

Completed

Conditions

Back Pain
Insomnia

Treatments

Device: Placebo Mattress Cover
Device: Active Mattress Cover

Study type

Interventional

Funder types

Other

Identifiers

NCT00969540
mattress1

Details and patient eligibility

About

Sleep quantity and quality can be influenced by the type of mattress used. This study is being done to see if a mattress cover with optically active particles can help back pain and improve sleep quality.

Full description

It is commonly observed that sleep in its quantity and quality is influenced by the type of mattress used at night. A recent study in patients with back pain showed that waterbeds and foam mattresses did influence back symptoms, function and sleep more positively than did a hard mattress. Pain improves with airbeds compared to regular innerspring mattresses. This study will analyze the effect of optically active particles mattress covers on sleep. The researcher is interested in learning if regular mattress or the study mattress cover (containing optically modified polyethylene terephthalate fiber mattress cover) is more useful in helping back pain and sleep quality.

Enrollment

8 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

You are eligible to participate in this study if you:

  • have a clinical diagnosis of chronic lower back pain
  • have pain measured on the Visual Analogue scale
  • have sleep disturbances at night associated with chronic lower back pain
  • are 18 years or older
  • sign the written, informed consent form prior to the initiation of any study procedures
  • have an habitual bedtime between 8 P.M. and 12 A.M.
  • are on a stable pain management regime

Exclusion criteria

You are not eligible to participate in this study if you:

  • are unwilling or unable to comply with the protocol or scheduled appointments
  • are unable to understand the language in which the approved informed consent is written
  • have no pain measured on the Visual Analogue scale
  • are unable to walk, wheel chair bound or confined to bed
  • are deemed by the investigator to be unreliable to wear the actigraphy, to complete the sleep log, to use the provided mattress covers at the proper time, to come to the scheduled visits or to answer questions regarding the subject's condition or medication use
  • lack a mobile arm to which to attach an actigraphy.
  • are currently participate or participated in another clinical study within the past 30 days
  • demonstrate an unwillingness to comply with the maximum limit of two alcoholic drinks per day and only 1 alcoholic drink after 6:00 P.M. for the duration of the protocol
  • use tobacco products or any other products during nightly awakenings that may interfere with the sleep wake cycle
  • have any unstable medical condition as determined by the investigator, or any other serious disease or condition that might affect life expectancy or make it difficult to successfully manage and follow the subject according to the protocol

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Triple Blind

8 participants in 2 patient groups, including a placebo group

Active Mattress Cover
Active Comparator group
Description:
Subjects in this arm will be given the placebo mattress cover followed active mattress cover .
Treatment:
Device: Active Mattress Cover
Placebo Mattress Cover
Placebo Comparator group
Description:
Subjects in this arm will be given the active mattress cover followed by the placebo mattress cover.
Treatment:
Device: Placebo Mattress Cover

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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