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Giving a voice to people with intellectual disability: can a redesigned questionnaire make self-reporting truly accessible?

NCT ID NCT05857592

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Aug 07, 2026 · Last updated Aug 07, 2026

Summary

This study explores whether a standard self-report questionnaire about daily living skills can be understood and completed meaningfully by adults with mild intellectual disability (IQ 55-85). Researchers will first test the original questionnaire, then use feedback to create a more accessible version and see if participants understand it better. The goal is to develop a tool that lets people with intellectual disability share their own views more accurately, rather than relying only on caregivers.

What this could mean

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

Active substance
Adapted version of the ABAS-3 self-report questionnaire
What this could lead to
If successful, this could lead to more inclusive and accurate self-report tools for people with intellectual disabilities, improving their involvement in assessments and care decisions.
What could go wrong
This is a small, early-stage study (20 participants) focused on understanding and feasibility, not on proving clinical effectiveness. Results may not generalize to all people with intellectual disabilities.

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

20 people

The number who actually took part.

Started

Jul 2023

Finished

May 2024

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: * Age 18 years or older * Last known Total Intelligence Quotient (TIQ) 55 - 85 * Receiving support from a care organization for persons with ID. * A care worker who knows the participant for at least a year and knows him well enough tot complete the informant version of the ABAS-3 is available. Exclusion Criteria: • Severe physical or sensory impairment limiting ability to participate.

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

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

Contacts and locations

Locations

  • Koraal

    Sittard, L, 6130 PC, Netherlands

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Other studies related to the condition(s) this trial covers.