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Bed scale could help wheelchair users shed pounds

NCT ID NCT07141342

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 24, 2026 · Last updated Jul 30, 2026 · Updated 4 times

Summary

This study tests a special bed scale that automatically weighs wheelchair users when they get in and out of bed. The goal is to help them lose weight by providing daily feedback, combined with a lifestyle program. About 92 adults who use wheelchairs and are overweight or obese will participate for 12 months.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
Fast In-Bed Tracking (FIT) System bed scale and Group Lifestyle Balance Adapted for Individuals with Impaired Mobility (GLB-AIM) behavioral program
What this could lead to
If successful, this could provide a convenient way for wheelchair users to track their weight daily, helping them lose weight and reduce obesity-related health risks.
What could go wrong
This is a small, early-stage trial with 92 participants, so results may not apply to all wheelchair users. The device only works for those who transfer in and out of bed, and weight loss success depends on user adherence.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

About 20 people

The number the study aims to enrol. It can still change while the study runs.

Started

Feb 2026

Expected to finish

Jul 2027

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 years and older

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Age18 + * Live within approximately 75 miles of Pittsburgh * Uses a wheelchair as primary means of locomotion * Currently transfers in and out of bed every night (or most nights) * Has been diagnosed as obese or overweight * Are interested in losing weight * BMI in the range of approximately 25 to 40; BMI range will be determined from published evidence for the primary diagnosis of the participant. For example, spinal cord injury /quadriplegic BMI range of approximately 22 to 40; for amputees it will be based on location and level of amputation, or if no diagnosis specific evidence exists, a BMI of approximately 25 to 40 will be used as a general guideline. * Own a smart phone, and have reliable internet and wifi connection * Are comfortable using exercise equipment like resistance bands or hand pedal exercisers * Are able and willing to engage in exercise of moderate intensity * Weight in bed including sleep partner is an estimated combined weight of 600 pounds or less * Does not have a regular way to weigh themselves, such as a roll-on scale in the home or gym, or have regular access to a device to weigh themselves regularly and are willing to avoid weighing themselves during the trial. * Indication that the participant has autonomy in decision-making as determined by the "Everyday Autonomy Self-Determination Scale." * Indication that their current bedroom setup is compatible with the FIT bed scales as determined by the "Bed Determination Survey." Due to the medical complexity of this population, inclusion of this study based on BMI, in-bed transfer frequency, or geographic location will be at the discretion of the expert members of our study team and will be considered on a case-by-case basis. Exclusion Criteria: * Extended vacations or absences planned in the next year (more that 2 - 4 weeks) or plans to move approximately 75 miles or greater from the Pittsburgh region * BMI outside of the desired range as based on condition and as determined by the study team. * Currently taking weight loss medication, medications that affect appetite, or have had weight loss surgery in the last 2 years. * History disordered eating in the last 2 years, such as Anorexia Nervosa, Bulimia Nervosa or Binge Eating Disorder * Currently pregnant or intend to become pregnant in the next 12 months * Regularly have 4 or more alcoholic drinks a day * Have any cognitive conditions that limit decision making or self-governing. * Indication that the participant does not have autonomy in decision-making as determined by the "Everyday Autonomy Self-Determination Scale." * Indication that their current bedroom setup is not compatible with the FIT bed scales as determined by the "Bed Determination Survey." Due to the medical complexity of this population, exclusion from this study based on BMI, geographic location, and what is considered a "medication that affects appetite" will be at the discretion of the expert members of our study team and will be considered on a case-by-case basis.

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Conditions

The condition(s) this trial relates to.

Obesity obesity disorder Overweight

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • University of Pittsburgh, Bakery Square, Department of Rehabilitation Science and Technology

    RECRUITING

    Pittsburgh, Pennsylvania, 15206, United States

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