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The effects of lifestyle counselling on anthropometric and body composition parameters in overweight/obese adults with HIV receiving first-line antiretroviral therapy: A randomized controlled trial

The effects of lifestyle counselling on anthropometric and body composition parameters in overweight/obese adults with HIV receiving first-line antiretroviral therapy: A randomized controlled trial

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
TCTR
Registry ID
TCTR20240905007
Enrollment
132
Registered
2024-09-05
Start date
2023-01-05
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

overweight or obesity lifestyle intervention, HIV, overweight, obesity, antiretroviral therapy

Interventions

The primary outcome of the study was the change in body weight and body composition at 6 months. Weight change was assessed as both the amount lost from baseline and the percentage of baseline body w
Experimental Behavioral,No Intervention No treatment
counselling group,control group

Sponsors

Addis Ababa University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. The study were enrolled PLWH with overweight or obese, aged 18-65 years 2. They had started combination antiretroviral therapy following the implementation of the test-and-treat strategy in Ethiopia and received antiretrovirals for at least 12 months 3. Maintained viral suppression, and were free of opportunistic infections during the intervention. 4. Eligible participants who had a baseline physical activity level of less than 600 metabolic equivalents in minutes per week

Exclusion criteria

Exclusion criteria: 1. The participants who had undergone formal dietary or physical activity counselling or engaged in organized nutritional and physical activity programs at baseline of the study. 2. Individuals with a history of pulmonary or cardiac complications, neurological problems, or musculoskeletal disorders were excluded from the study. 3. The individuals with confirmed thyroid disease, uncontrolled hypertension, physical conditions that restrict the ability to engage in physical activity, pregnancy at any point during the study, and those with chronic liver and/or renal diseases. 4. Additionally, participants who are undergoing lent or other fasting practices at any point during the study and those failing to meet the inclusion criteria were also excluded.

Design outcomes

Primary

MeasureTime frame
weight loss and change in body composition at baseline and after 6 months by using previously validated bioelectrical impedance(BIA). BIA was employed via an Omron Body Composition Monitor with Scale (Omron HBF-514C analyzer, Omron healthcare Inc., Japan)

Secondary

MeasureTime frame
at least 3% weight loss at baseline and after 6 months percent weight loss: ([weight at 6 months minus weight at baseline]/weight at baseline)x100

Countries

Ethiopia

Contacts

Public ContactAgete Tadewos Hirigo

Hawassa University

agetetadewos@yahoo.com0913175126

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026