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Behavioral Intervention

Mindfulness Based Stress Reduction for Human Immunodeficiency Virus Infection

N/A

Waitlist Available

Research Sponsored by University of Alabama at Birmingham

Eligibility Criteria Checklist

Specific guidelines that determine who can or cannot participate in a clinical trial

Must have

Be older than 18 years old

Timeline

Screening 3 weeks

Treatment Varies

Follow Up immediately post-intervention or 8 weeks.

Awards & highlights

Study Summary

This trial aims to reduce stress and improve HIV self-care in black women living with HIV, in order to help attenuate the racial and gender disparities in HIV care in the US.

Eligible Conditions

Human Immunodeficiency Virus (HIV) Infection
Health Behaviors

Timeline

Screening ~ 3 weeks3 visits

Treatment ~ Varies

Follow Up ~ immediately after the intervention(which consists of an orientation followed by eight weekly sessions, consistent with msbr interventions), the measure was collected within one week of completing the final session.

Screening ~ 3 weeks

Treatment ~ Varies

Follow Up ~immediately after the intervention(which consists of an orientation followed by eight weekly sessions, consistent with msbr interventions), the measure was collected within one week of completing the final session.

This trial's timeline: 3 weeks for screening, Varies for treatment, and immediately after the intervention(which consists of an orientation followed by eight weekly sessions, consistent with msbr interventions), the measure was collected within one week of completing the final session. for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.

Primary outcome measures

Feasibility Intervention Measure

Secondary outcome measures

Mindfulness

Social support

Trial Design

2Treatment groups

Active Control

Group I: Mindfulness Based Stress ReductionActive Control1 Intervention

MBSR sessions received by the treatment group will include an orientation, approximately 8 intervention sessions, and an exit interview.

Group II: Standard of CareActive Control1 Intervention

The control condition will continue receiving usual care or standard of care.

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Who is running the clinical trial?

University of Alabama at BirminghamLead Sponsor

1,588 Previous Clinical Trials

2,280,264 Total Patients Enrolled

National Center for Complementary and Integrative Health (NCCIH)NIH

832 Previous Clinical Trials

668,885 Total Patients Enrolled

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Is the enrollment period for this experiment still open?

"Affirmative. Clinicaltrials.gov reveals that this clinical trial is still recruiting individuals, having initially been posted on February 11th 2022 and edited most recently on November 7th 2022. The research team are looking to enlist 48 participants from one medical centre."

Answered by AI

What is the cap placed on participant numbers for this experiment?

"Affirmative, according to clinicaltrials.gov the trial first went public on February 11th 2022 and was recently revised on November 7th 2022. This study requires 48 individuals from one location to join."

Answered by AI

Recent research and studies

clinicaltrials.govStudy

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

Crystal C. Lambert 2022. "Feasibility of the Mindfulness-Based Stress Reduction Intervention for Black Women Living With HIV". ClinicalTrials.gov. https://clinicaltrials.gov/ct2/show/NCT04193605.