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Optimizing Resilience and Coping in HIV Via Internet Delivery

Not Applicable
Completed
Conditions
Depression
Psychological Stress
HIV Disease
Affect
Interventions
Behavioral: Intervention
Registration Number
NCT01997008
Lead Sponsor
University of California, San Francisco
Brief Summary

This is a feasibility/pilot test of a set of positive affect skills provided online to HIV positive people with elevated depressive symptoms - a Center for Epidemiological Studies Depression Scale D (CES-D) score \> 10. The investigators will test the feasibility of recruitment, retention and acceptability of these skills in an online delivery format, determine feasibility and acceptability of daily emotion assessments via text messaging and assess efficacy of these skills for improving psychological well-being this population.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
22
Inclusion Criteria
  • HIV +
  • 18 or older
  • Score of CES-D depression scale >10
  • Daily internet access
  • Smart phone ownership
Read More
Exclusion Criteria
Read More

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
InterventionInterventionParticipants receive a five week intervention providing the following activities: EMA: Ecological Momentary Assessment (EMA) of Emotion throughout the day. Intervention: Positive Events: Participants identify a positive event and then describe how they capitalized on this event. Gratitude: Participants identify one more more things that make them feel grateful. Mindfulness: Participants participate in a 30 minute guided mindfulness/meditation practice. Positive Reappraisal: Participants identify how they reappraised a negative event making it into a positive event. Personal Strengths: Participants identify one more more personal strengths. Attainable goals: Participants identify a short-term attainable goal. Participants will outline what they did that day to work toward attaining their week's goal. Acts of Kindness: Participants will identify one more more acts of kindness that they engaged in and how it made them feel.
Primary Outcome Measures
NameTimeMethod
Retention of participants in online delivery format.5 weeks post enrollment. May be slightly more or less for intervention participants depending on time taken to complete online content.

We will track, for each participant who completes a screening questionnaire, where they heard about the study and the proportion who go on to enroll. We will track retention - noting when participants drop out to determine if particular sessions or activities result in less retention than other areas.

Acceptability of ORCHID content5 weeks post enrollment. May be slightly more or less for intervention participants depending on time taken to complete online content.

We will track participation in both the self-report questionnaires as well as the intervention sessions (e.g., number of ORCHID sessions completed, amount of home practice completed). We will carefully track usage - noting when participants who leave the study drop out to determine if there are particular sessions that are less acceptable than others.

Feasibility of an online delivery format.5 weeks post enrollment. May be slightly more or less for intervention participants depending on time taken to complete online content.

We will follow up with participants who have significant missing data to determine areas in which the protocol is feasible and to highlight areas for improvements. We will summarize participant feedback regarding the protocol and will use this feedback to inform the subsequent proposals.

Secondary Outcome Measures
NameTimeMethod
Determine acceptability of multiple daily emotion assessments using text messaging.5 weeks post enrollment. May be slightly more or less for intervention participants depending on time taken to complete online content.

To measure this outcome, we will first document if anyone declines participation due to the perceived burden of the Ecological Momentary Assessment (EMA) protocol. We will carefully document adherence to the protocol and the proportion of assessments that participants complete. In the follow-up interviews, we will have questions specific to the EMA protocol to elicit feedback and suggestions for improvement

Trial Locations

Locations (1)

University of California, San Francisco

🇺🇸

San Francisco, California, United States

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