Effects of Mattress Firmness on Pain in Patients With Chronic Low-Back Pain

NCT ID: NCT01044121

Last Updated: 2013-01-10

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

TERMINATED

Clinical Phase

NA

Total Enrollment

40 participants

Study Classification

INTERVENTIONAL

Study Start Date

2010-01-31

Study Completion Date

2012-07-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The primary study objective is to determine whether mattress firmness affects pain in patients with chronic low-back pain. We hypothesize that mattresses that differ in their firmness and support should have a varying effect on low-back pain patients' level of pain and pain-related disability. We also seek to test the hypothesis that the optimal mattress might vary from person to person.

In this regard, we will test:

1. Whether there is a single mattress that is superior to the others in terms of reducing low-back pain and pain related disability.
2. Whether the optimal mattress for reducing pain varies in the observed population.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Few treatments are effective for chronic low-back pain, a disorder that causes marked social costs in developed countries. A "comfortable" mattress is commonly assumed to play an essential role, both on a preventive and on a therapeutic basis on chronic low-back pain. However, evidence supporting the beneficial effects of different levels of mattress support on pain is lacking.

The primary study objective is to determine whether mattress firmness affects pain in patients with chronic low-back pain. We hypothesize that mattresses that differ in their firmness and support should have a varying effects on LBP patients' level of pain and pain-related disability. We also seek to test the hypothesis that the optimal mattress might vary from person to person. In this regard, we will test:

1. whether there is a single mattress that is superior to the others in terms of reducing low-back pain and pain-related disability and
2. whether the optimal mattress for reducing pain varies in the observed population.

The secondary objectives are:

1. to determine whether there is a relationship between mattress firmness and sleep in this population;
2. to determine whether there is a relationship between pain and sleep in this population;
3. to determine whether key sleep variables (subjective or objective) are mediating or moderating factors of the relationship between mattress and level of low-back pain (LBP) and disability;
4. to determine if different sleep surfaces have differential effects on measures of daily function among patients with chronic LBP;
5. to evaluate if Kingsdown's proprietary algorithm for selecting optimal mattress "fits" with the subject's best mattress for reducing pain and improving sleep and measures of daytime functioning;
6. to conduct exploratory regression analyses using variables included in the proprietary algorithm and other demographics and measures of physical characteristics to predict the optimal "fit" mattress (i.e., the mattress associated with lowest morning pain ratings, best sleep measures and optimal levels of daytime function);
7. to determine if different sleep surfaces have differential effects on measures of partner sleep disturbance;
8. to determine if there is a relationship between partner pain level and partner sleep disturbances.

Please see "Eligibility Criteria" for inclusion and exclusion information.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Low Back Pain Sleep Disruption

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Intervention Model

CROSSOVER

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

SINGLE

Participants

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Mattress Firmness

Group Type EXPERIMENTAL

Mattress Firmness

Intervention Type OTHER

Current mattress and 6 experimental firmnesses of mattress as defined by a Comfort Support Analysis device.

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Mattress Firmness

Current mattress and 6 experimental firmnesses of mattress as defined by a Comfort Support Analysis device.

Intervention Type OTHER

Other Intervention Names

Discover alternative or legacy names that may be used to describe the listed interventions across different sources.

Kingsdown Sleep to Live

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Low back pain location must be inferior to T12 and superior to the gluteal fold and chronic (greater than 3 months)
* Patient Global Impression for Pain of at least 3 on a 1-5 scale (moderate severity)
* Visual Analog Scale for Pain of at least 40 on a 100 point scale (0 = no pain; 100 = worst pain)
* Presence of normal motor strength on exam
* English speaking and reading man/woman between the ages of 21-64

Exclusion Criteria

* Neurologic or medical illness that is directly responsible for back pain
* Psychiatric disease
* Back related surgery
* Substance abuse
* Pregnancy (self or partner)
* Sleep-affecting medications
* Recent surgery
* Recent physical trauma
* Fibromyalgia
* Spinal Stenosis
* Sciatica
* Spondylolisthesis
* Spondyloarthropathy
* Sciatica
* Spinal Stenosis
* Vertebral Fractures
* Rheumatoid Arthritis
* Inability to comply
* Untreated sleep disorders
* Night-shift worker
* Frequent travel
* Parent of child under 2
* Pending litigation for pain issue
* Corticosteroid use in the last 90 days
Minimum Eligible Age

21 Years

Maximum Eligible Age

64 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Duke University

OTHER

Sponsor Role collaborator

Sleep To Live Institute

INDUSTRY

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Robert Oexman, DC

Role: PRINCIPAL_INVESTIGATOR

Sleep To Live Institute

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

Duke-Pain-1113291

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Pain Resilience for Low Back Pain.
NCT06971809 ENROLLING_BY_INVITATION NA
Effect of Massage on Chronic Low Back Pain
NCT00371384 COMPLETED PHASE2/PHASE3
Thoraco-Lumbar Fascia Mobility
NCT03916705 COMPLETED NA