Examining the Feasibility and Acceptability of a Tailored Version of a Mindfulness-Based Intervention (MBI) Among Youth Experiencing Homelessness (YEH)
CompletedNAResults postedLast updated 28 August 2025
What this trial tests
NA trial testing tailored MBI (.b) in Stress, Emotional in 90 participants. Completed in 8 June 2024.
Timeline
28 March 2022
Primary endpoint 8 June 2024
8 June 2024
Quick facts
Lead sponsor
The University of Texas Health Science Center, Houston
The University of Texas Health Science Center, Houston
Who can join
Adults 18 to 25, any sex, with Stress, Emotional. Patients with the condition only — healthy volunteers not accepted.
Results — posted to ClinicalTrials.gov
Per-arm endpoint measurements with 95% confidence intervals where reported. Source: trial results section.
Emotion Regulation as Measured by Difficulties in Emotion Regulation Scale (DERS)Primary· Baseline
The DERS is a 36-item questionnaire, and each item is scored from 1(almost never)-5 (almost always). The 36 items were added to generate a scale from 36 to 180, a higher score indicates greater problem with emotion regulation.
Group
Value
95% CI
Tailored MBI (.b)
93.18
± 26.41
Attention Control Condition
82.62
± 23.42
Emotion Regulation as Measured by Difficulties in Emotion Regulation Scale (DERS)Primary· immediately after completing the intervention (about 2 to 4 weeks after baseline)
The DERS is a 36-item questionnaire, and each item is scored from 1(almost never)-5 (almost always). The 36 items were added to generate a scale from 36 to 180, a higher score indicates greater problem with emotion regulation.
Group
Value
95% CI
Tailored MBI (.b)
86.03
± 21.82
Attention Control Condition
94.74
± 21.19
Emotion Regulation as Measured by Difficulties in Emotion Regulation Scale (DERS)Primary· 3 months post intervention
The DERS is a 36-item questionnaire, and each item is scored from 1(almost never)-5 (almost always). The 36 items were added to generate a scale from 36 to 180, a higher score indicates greater problem with emotion regulation.
Group
Value
95% CI
Tailored MBI (.b)
85.4
± 22.25
Attention Control Condition
91.56
± 19.64
Emotion Regulation as Measured by Difficulties in Emotion Regulation Scale (DERS)Primary· 6 months post intervention
The DERS is a 36-item questionnaire, and each item is scored from 1(almost never)-5 (almost always). The 36 items were added to generate a scale from 36 to 180, a higher score indicates greater problem with emotion regulation.
Group
Value
95% CI
Tailored MBI (.b)
90.36
± 24.21
Attention Control Condition
94.26
± 17.17
Mindfulness as Measured by Child and Adolescent Mindfulness Measure (CAMM)Primary· Baseline
The CAMM is a 10 item questionnaire and each item is scored from 0(never true)-4 (always true). The 10 items were added to generate a scale from 0 to 40, a higher score indicates higher levels of mindfulness
Group
Value
95% CI
Tailored MBI (.b)
23.84
± 9.3
Attention Control Condition
27.38
± 11.26
Mindfulness as Measured by Child and Adolescent Mindfulness Measure (CAMM)Primary· immediately after completing the intervention (about 2 to 4 weeks after baseline)
The CAMM is a 10 item questionnaire and each item is scored from 0(never true)-4 (always true). The 10 items were added to generate a scale from 0 to 40, a higher score indicates higher levels of mindfulness
Group
Value
95% CI
Tailored MBI (.b)
26.89
± 9.47
Attention Control Condition
24.31
± 10.41
Mindfulness as Measured by Child and Adolescent Mindfulness Measure (CAMM)Primary· 3 months post intervention
The CAMM is a 10 item questionnaire and each item is scored from 0(never true)-4 (always true). The 10 items were added to generate a scale from 0 to 40, a higher score indicates higher levels of mindfulness
Group
Value
95% CI
Tailored MBI (.b)
28.73
± 9.08
Attention Control Condition
27.74
± 10.61
Mindfulness as Measured by Child and Adolescent Mindfulness Measure (CAMM)Primary· 6 months post intervention
The CAMM is a 10 item questionnaire and each item is scored from 0(never true)-4 (always true). The 10 items were added to generate a scale from 0 to 40, a higher score indicates higher levels of mindfulness
Group
Value
95% CI
Tailored MBI (.b)
25.92
± 9.2
Attention Control Condition
30.36
± 9.39
Self-Compassion as Measured by Self-Compassion Scale (SCS)Primary· Baseline
The Self-Compassion Scale (SCS) total score ranges from 1 to 5, higher score indicating greater self compassion..
Group
Value
95% CI
Tailored MBI (.b)
3.06
± 0.47
Attention Control Condition
3.21
± 0.44
Self-Compassion as Measured by Self-Compassion Scale (SCS)Primary· immediately after completing the intervention (about 2 to 4 weeks after baseline)
The Self-Compassion Scale (SCS) total score ranges from 1 to 5, higher score indicating greater self compassion.
Group
Value
95% CI
Tailored MBI (.b)
3.11
± 0.60
Attention Control Condition
3.05
± 0.33
Self-Compassion as Measured by Self-Compassion Scale (SCS)Primary· 3 months post intervention
The Self-Compassion Scale (SCS) total score ranges from 1 to 5, higher score indicating greater self compassion.
Group
Value
95% CI
Tailored MBI (.b)
3.20
± 0.60
Attention Control Condition
3.15
± 0.37
Self-Compassion as Measured by Self-Compassion Scale (SCS)Primary· 6 months post intervention
The Self-Compassion Scale (SCS) total score ranges from 1 to 5, higher score indicating greater self compassion.
Group
Value
95% CI
Tailored MBI (.b)
3.23
± 0.43
Attention Control Condition
3.06
± 0.25
Sponsor's own description
The purpose of this study is to conduct a trial of the tailored Mindfulness- Based Intervention (MBI) (.b) vs. attention control to test real-world feasibility and acceptability of this tailored Mindfulness - Based Intervention (MBI) in youth experiencing homelessness (YEH).
Publications & conference data
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
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Sponsor: as reported to ClinicalTrials.gov by The University of Texas Health Science Center, Houston
Last refreshed: 28 August 2025
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04950816.