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Readiness to Disclose Mother's HIV Diagnosis to Their Children in Beijing, China

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Yale University

Status

Completed

Conditions

HIV

Treatments

Behavioral: disclosure-support counseling intervention

Study type

Interventional

Funder types

Other

Identifiers

NCT03248778
2000020567

Details and patient eligibility

About

Specific aims of the 1-year project are to pilot test the disclosure support intervention by (a) evaluating acceptability and feasibility with a preliminary randomized trial among 10 HIV+ mothers (5 in the intervention group and 5 in the treatment as usual (TAU) group) and (b) assessing outcomes in mothers (quality of life and mental health indicators, adherence, social support, and disclosure stress, efficacy, readiness, and completion). The intervention will be compared to treatment as usual, with baseline (0 weeks), immediate post-intervention (4 weeks), and 12-week follow-up (16 weeks) assessments.

Full description

HIV disclosure to children has been shown to strengthen family relations and increase assistance with medical care, reinforcing the parent's willingness to live. Some Chinese children aware of their parents HIV diagnosis do exhibit emotional and social dysfunction; however, adequate support from caregivers (e.g., grandparents or even their HIV+ parents) can improve the children's quality of life and academic performance. There is a clear need for practical interventions to address parental distress around HIV disclosure in China, where cultural norms often emphasize family identity and cohesion and underscore the need for family-based programs, which have been shown to be feasible and efficacious for HIV-affected families.

Enrollment

5 patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • HIV+ mother ≥18 years of age,
  • not psychotic or demented;
  • receiving clinical care at the Ditan hospital,
  • a mother of an HIV-negative child of age 13-25 years who does not know about the mother's infection;
  • well enough to attend study sessions as the clinic.

Exclusion criteria

  • no psychotic or demented

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

5 participants in 2 patient groups

disclosure-support counseling
Experimental group
Treatment:
Behavioral: disclosure-support counseling intervention
Treatment as Usual
No Intervention group

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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