MedDataX Logo

Phone Call in Type 2 Diabetes Patient

NCT ID: NCT00810173

Last Updated: 2008-12-17

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

48 participants

Study Classification

INTERVENTIONAL

Study Start Date

2008-01-31

Study Completion Date

2008-10-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

To assay the influence of personality profile to promote behavior change adherence for physical activity using a pedometer. The investigators also studied the metabolic profile, diagnosis of depression, intention to change behavior, physical activity referred and the quality of life. Casuistic and Methods: a randomized "quasi-experimental" enrolling 48 T2DM patients using a pedometer for 6 weeks. The intervention group received phone calls stimulating them to increase their walking activity. The control group received only one telephone call to explain pedometer use. The investigators also analyzed the personality profile, quality of life, and metabolic and anthropometric indexes.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Behavior Change

Keywords

Explore important study keywords that can help with search, categorization, and topic discovery.

type 2 diabetes physical activity behavior change profile personality phone call support

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

NONE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

1

This group received call phone support to incentive the increase of the number of steps during 6 weeks

Group Type EXPERIMENTAL

phone call support

Intervention Type BEHAVIORAL

The intervention group received a phone call support for 6 weeks to incentive to increase the number of steps/day.

2

This group just received a pedometer to register the number of steps for 6 weeks but this group don´t received a phone call.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

phone call support

The intervention group received a phone call support for 6 weeks to incentive to increase the number of steps/day.

Intervention Type BEHAVIORAL

Other Intervention Names

Discover alternative or legacy names that may be used to describe the listed interventions across different sources.

couselling to behavior change

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* to assign written informed consent
* to have a phone call number
* to agree to use a pedometer for 6 weeks to be able to write the data concerning their number of steps per day

Exclusion Criteria

* don´t agree to assign written informed consent
* don´t have phone number
* don´t have conditions to answer all the questionnaire
* don´t agree to use pedometer for 6 weeks
Minimum Eligible Age

40 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

University of Sao Paulo

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Hospital das Clínicas da Universidade de São Paulo

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

Fonseca-Guedes

Identifier Type: -

Identifier Source: org_study_id