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Behavioral intervention about adherence to oral antidiabetic to treatment of diabetes mellitus

Effect of strategies "action planning and coping planning" about adherence to oral antidiabetic agents: a randomized clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-439f77
Enrollment
Unknown
Registered
2016-01-12
Start date
2016-01-11
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

diabetes mellitus type 2, medication adherence, hypoglycemic agents, stress psychological

Interventions

Experimental group: Application of strategies "action planning and coping planning". Frequency: on the 15th and 60th days after recruitment and telephone reinforcement on the 30th and 75th days after

Sponsors

Faculdade de Enfermagem da Universidade Estadual de Campinas - Unicamp
Lead Sponsor
Faculdade de Enfermagem da Universidade Estadual de Campinas - Unicamp
Collaborator

Eligibility

Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: Patients of both genders with diabetes mellitus,type 2; adults over 18 years; continuous use for at least six months of oral antidiabetic agents; show an average score intention greater than or equal to 4.

Exclusion criteria

Exclusion criteria: Drug administration by a caregiver; use insulin to treat diabetes mellitus; make diabetes monitoring in other health service.

Design outcomes

Primary

MeasureTime frame
Increasing the taking and overall proportion of adherence to oral antidiabetic agents in more than 80%,determined through the action planning strategies and coping planning strategies from the realization of a range of at least 5% in the study beginning and end of the study. ;Decrease in glycated hemoglobin value in the period of 105 days, determined through the action planning strategies and coping planning strategies from the realization of a range of at least 5% in the study beginning and end of the study. Decrease emotional distress related to diabetes in the period of 105 days, determined through the action planning strategies and coping planning strategies from the realization of a range of at least 5% in the study beginning and end of the study.

Secondary

MeasureTime frame
Decrease emotional distress related to diabetes in the period of 105 days, determined through the action planning strategies and coping planning strategies from the realization of a range of at least 5% in the study beginning and end of the study.;Maintenance or increase of behavioral intention, determined through the action planning strategies and coping planning strategies from the realization of a range of at least 5% in the study beginning and end of the study.

Countries

Brazil

Contacts

Public ContactDanilo;Maria Helena Trevisan;Lima

Faculdade de Enfermagem da Universidade Estadual de Campinas - Unicamp;Faculdade de Enfermagem da Universidade Estadual de Campinas - Unicamp

ddtrevisan@gmail.com;mhmelolima@gmail.com+55(19)35218836;+55(19)35218836

Outcome results

None listed

Source: REBEC (via WHO ICTRP)