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Clinical Trials/NCT00180700
NCT00180700
Completed
N/A

The Effects of Two Psychological Intervention Techniques, Self-hypnosis and Johrei Healing Method, on Quality of Life, Psychological Well-being, EEG Measures and Various Immunological Measures Including CD4+ Counts in Early HIV: a Randomly Controlled Pilot Study

Imperial College London1 site in 1 country22 target enrollmentJune 1, 2003

Overview

Phase
N/A
Intervention
Not specified
Conditions
HIV Infected Individuals
Sponsor
Imperial College London
Enrollment
22
Locations
1
Primary Endpoint
CD4 T-cell counts
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

This study examines the hypothesis that psychological interventions have beneficial effects on quality of life including psychological well-being and disease progression in early HIV patients recieving no medication.

Detailed Description

Hypothesis: This investigation is based upon the hypothesis that psychological intervention may counteract the detrimental effects of stress both on psychological well-being and on general health. Background: HIV infection may be considered to be a life-long biological and psychological stressor leading to detrimental outcomes associated with disease progression. Stress reduction in these patients may have beneficial effects through delaying disease progression via the proposed interactive psycho-neuro-endocrine-immune network. Inclusion Criteria: HIV infected individuals CD4 T-cell counts above 200 cells/mcl Receiving no anti-retroviral drugs Individuals who signed the informed consent form Investigative approach: Self-hypnosis and a Japanese non-touching, laying-on-of hands-like technique, called Johrei, were used to investigate the effects of psychological intervention upon immune parameters (especially in CD4 counts) associated with disease progression along with phenomenological associations between stress perception and stress hormone levels in HIV-infected patients receiving no medication.

Registry
clinicaltrials.gov
Start Date
June 1, 2003
End Date
December 1, 2003
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • HIV infected
  • CD4 T-cell counts above 200 cells/mcl
  • Signed the informed consent form

Exclusion Criteria

  • receiving anti-retroviral drugs

Outcomes

Primary Outcomes

CD4 T-cell counts

Time Frame: 4 weeks

Lab test

Secondary Outcomes

  • Endogenous hormone levels (cortisol, DHEA-S and melatonin)(4 weeks)
  • Other immunological parameters (Viral load levels, NK cell counts)(4 weeks)
  • Psychological questionnaires (Perceived Stress Scale (PSS), STAI, Beck depression Inventory (BDI))(4 weeks)

Study Sites (1)

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