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Effects of telephone use to promote the health of people living with HIV/AIDS

Effects of a telephone follow-up program to promote the health of people living with HIV/aids

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-86yn4b
Enrollment
Unknown
Registered
2017-07-10
Start date
2016-07-15
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Acquired Immunodeficiency Syndrome

Interventions

Intervention 1: Synchronous telephone monitoring - Telephone calls. This group will consist of 54 people living with HIV who will receive phone calls every fortnight for eight months. For each phone c
physical activity
Social relationship
self esteem
Anxiety and depression and self-esteem
Practice of preventive behavior and sexuality. Intervention 2: Asynchronous telephone monitoring - Telephone messages. This group will consist of 54 people living with HIV who will receive telephone m
Practice of preventive behavior and sexuality. Control: This group will consist of 54 people living with HIV who will receive the usual care of the service.
Behavioural
D013689
D060145

Sponsors

Departamento de Enfermagem da Universidade Federal do Ceará
Lead Sponsor
Departamento de Enfermagem da Universidade Federal do Ceará
Collaborator

Eligibility

Age
18 Years to 59 Years

Inclusion criteria

Inclusion criteria: Adults being treated for HIV; Both genders;age between 18 and 59 years.

Exclusion criteria

Exclusion criteria: Diminished visual acuity; dysarthria; accused; Mental disorder.

Design outcomes

Primary

MeasureTime frame
Increase in treatment adherence scores in the 18-month period verified by means of the instrument for assessing the degree of difficulty for adherence, based on a variation of at least 5% in pre and post-intervention measurements.The instrument for assessing the degree of adherence will be applied 6, 12 and 18 months after the intervention. Increase in quality of life scores in the 18-month period verified by means of the instrument for assessment of quality of life (HATQoL), based on the observation of a variation of at least 5% in pre and post intervention measurements.The quality of life instrument will be applied 6, 12 and 18 months after the intervention. Decreased symptoms suggestive of anxiety and depression in the 18-month period verified by means of the anxiety and depression scale (ADH), from the observation of a variation of at least 5% in the pre- and post-intervention measurements.The anxiety and depression scale will be applied 6, 12 and 18 months after the intervention. Increase in self-esteem scores in the 18-month period verified by the Rosemberg self-esteem scale (EAR), based on the observation of a variation of at least 5% in pre and post-intervention measurements.The self-esteem scale will be applied 6, 12 and 18 months after the intervention. Increase in lifestyle scores in the 18-month period verified by means of the instrument to evaluate the individual lifestyle profile, based on the observation of a variation of at least 5% in the pre and post intervention measurements.The instrument for evaluating the individual lifestyle profile will be applied 6, 12 and 18 months after the intervention.

Secondary

MeasureTime frame
Secondary outcomes are not expected

Countries

Brazil

Contacts

Public ContactMarli Teresinha Galvão

Departamento de Enfermagem da Universidade Federal do Ceará

marligalvao@gmail.com+55(85)3366 8455

Outcome results

None listed

Source: REBEC (via WHO ICTRP)