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RecruitingNCT07168941Updated Aug 28, 2026

Evaluation and Refinement of KF-STRIDE Into the Interview!

An interventional study of KF-STRIDE in Autism Spectrum Disorder, sponsored by Kessler Foundation. Recruiting at 1 site in United States. Open to participants aged 18 Years to 65 Years. Per ClinicalTrials.gov, last updated 2026-08-28.

Sponsored by Kessler Foundation · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Started Jan 2026; still recruiting 9 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
30
Allocation
Randomized
Ages
18 Years to 65 Years
Sex
All
01

Study summary

Examine the acceptability, usability, feasibility, and initial efficacy of KF-STRIDE 3.0, the data from which will serve as a basis for a future fully powered RCT

Read the detailed description

Although KF-STRIDE 2.0 was designed to support youth on the spectrum, its current design may not be appropriate for adults. Thus, the current proposal will support development activities to significantly adapt KF-STRIDE 2.0 to meet the specific needs of adults with autism. As part of development, the investigators will partner with the autism community, using mixed methodology to ensure the investigators' modifications are performed with community-engaged methods. The investigators will invite adults with autism, family members, employers, and vocational counselors to provide feedback to guide the modifications to KF-STRIDE. The investigators will then test the acceptability, feasibility, fidelity, and initial efficacy of KF-STRIDE 3.0 among adults on the spectrum. Obtaining employment is essential to individuals on the spectrum as it can lead to improved community integration, increased social networking, and a means to contribute to society as productive citizens. Overall, the investigators propose to adapt a treatment that has strong potential to help adults with autism improve their job interview skills that will lead to increased employment.

02

Conditions studied

  • Autism Spectrum Disorder
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In context

Autism Spectrum Disorder

1,724 studies on the registry are indexed under Autism Spectrum Disorder; 500 are open to participants now.

This study's planned enrollment of 30 is below the median of 52 across 1,368 interventional studies indexed under Autism Spectrum Disorder.

Browse Autism Spectrum Disorder studies →

Lead sponsor

Kessler Foundation is the lead sponsor of 175 studies on the registry; 61 are open to participants now.

Of its 5 completed or terminated interventional studies of FDA-regulated products, 0 (0%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Participants live in the United States of America
  • Participants speak English Fluently and at a 4th grade reading level

Exclusion criteria

Exclusion Criteria:

  • Participants have a history of significant psychiatric illness (like bipolar disorder, schizophrenia, or psychosis)
  • Participants have a history of substance abuse
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
30 participants (estimated)

Study arms

  • Experimental
    Kessler Foundation STRength IDentification and Expression (KF-STRIDE)

    Behavioral: KF-STRIDE

  • No intervention
    Services as Usual

Interventions

  • BehavioralKF-STRIDE

    KF Stride works to improve identification (awareness) of personal character strengths and 2) express them in a socially appropriate way during a job interview

06

What researchers measure

Primary outcomes

  1. 20-minute long video-recorded Mock Job Interview, Autism Mock Interview Rating-Scale(A-MIRS)

    Participants will choose 1 of 7 possible employment positions (i.e., security, childcare, culinary arts). Digital recordings will be scored by blinded raters with human resources expertise and trained to a reliable standard. Briefly, raters will rate videos using the Autism Mock Interview Rating-Scale (A-MIRS). The A-MIRS will rate the participant's 'likeliness to be hired' along with different interview skills (using a Likert-type scale 1=Poor to 7=Excellent). A total score will be evaluated, with higher scores indicating a higher likelihood to be hired. Maximum score of 77 and minimum score of 11. A higher score indicated better performance.

    Time frame: Baseline, Immediate Post-Test between weeks 7 and 8

  2. Work Readiness Scale

    13 items about the perception of one's ability to work, with values ranging from 1 (strongly disagree) to 5(strongly agree), with higher scores indicating more work readiness. The maximum score is 65 and the minimum score is 13. A higher score indicates a better work readiness outcome.

    Time frame: Baseline, Immediate Post-Test between weeks 7 and 8

  3. Employment Status

    The investigators will examine whether the participant became employed or other changes to employment status, (employment status, hours worked, wages earned, etc.) . Yes=1, No=0

    Time frame: Baseline, Immediate Post-Test between weeks 7 and 8

Secondary outcomes

  1. World Health Organization Quality of Life abbreviated version (WHOQOL-BREF)

    A self-report questionnaire which assesses 4 domains of quality of life (QOL): physical health, psychological health, social relationships, and environment. The range of scores is between 26 (minimum) and 130 (maximum). Higher scores indicate better quality of life.

    Time frame: Baseline, Immediate Post-Test between weeks 7 and 8

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Study locations

1 of 1 sites recruiting
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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Jan 2026 (actual). Primary completion is estimated for Jan 2027, 11 months after the start.

Of 800 non-industry interventional studies with no phase under Autism Spectrum Disorder, half reached primary completion within 25 months of starting (the median), counting those still running; a quarter within 12 and three quarters within 48. This study's planned 11 months is below that.

Counting every sponsor, half of 823 studies reached it within 25 months; a quarter within 12 and three quarters within 47.

How these figures are worked out, and which studies are left out of them.

Registered
Sep 4, 2025
First posted
Sep 11, 2025
StartActual
Jan 26, 2026
Primary completionEst.
Jan 1, 2027
CompletionEst.
Jul 1, 2027
Last update
Aug 28, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Aug 28, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07168941
Lead sponsor
Kessler Foundation
Responsible party
Helen Genova (Associate Director, Kessler Foundation) — Principal investigator
First posted
Sep 11, 2025
Start date
Jan 26, 2026
Primary completion
Jan 1, 2027 (estimated)
Completion
Jul 1, 2027 (estimated)
Last update
Aug 28, 2026

Study contacts

Helen Genova
Contact
hgenova@kesslerfoundation.org
973-324-8390
Michael Dacanay
Contact
mdacanay@kesslerfoundation.org
973-324-8453

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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