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Feasibility of the Mindfulness-Based Stress Reduction Intervention for Black Women Living With HIV Supplement

The University of Alabama at Birmingham logo

The University of Alabama at Birmingham

Status

Completed

Conditions

Mild Cognitive Impairment
HIV Infections

Treatments

Other: Usual Care
Behavioral: Mindfulness

Study type

Interventional

Funder types

Other

Identifiers

NCT04984681
K23AT010567 (U.S. NIH Grant/Contract)
K23AT010567S

Details and patient eligibility

About

In our Supplement Aim we will conduct a two-arm randomized pilot test of the adapted intervention compared to a usual care control group among 30 African American/Black women with HIV (15/arm) to assess the feasibility and acceptability of the mindfulness-based stress reduction among women with HIV with mild cognitive impairment. Feasibility will be assessed by our ability to (1) recruit, randomize, and retain participants and (2) deliver the intervention per the manual, as well as (3) participants adherence to home practices and assignments. Acceptability will be assessed via qualitative data (focus group input regarding participants' satisfaction with the intervention and intent to continue using the practices), as well quantitative data (satisfaction survey).

Enrollment

30 patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Cisgender females
  • HIV seropositive
  • 18 years of age or older
  • English speaking
  • An active patient at the local HIV ambulatory clinic in Alabama.
  • No history of neurological (including dementia diagnosis)
  • No history of severe psychiatric (e.g., schizophrenia or bipolar disorder) disorders

Exclusion criteria

  • Non-English speaking
  • Appear temporarily impaired (e.g., intoxicated)
  • Not willing to or legally unable to provide informed consent.

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

30 participants in 2 patient groups

Mindfulness-based Stress Reduction
Experimental group
Description:
Mindfulness-based stress reduction sessions received by the treatment group will include an orientation, approximately 8 intervention sessions, and an exit interview.
Treatment:
Behavioral: Mindfulness
Usual Care
Other group
Description:
The control condition will continue receiving usual care or standard of care.
Treatment:
Other: Usual Care

Trial documents
1

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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