Phone Call in Type 2 Diabetes Patient

Sponsor
University of Sao Paulo (Other)
Overall Status
Completed
CT.gov ID
NCT00810173
Collaborator
(none)
48
2
9

Study Details

Study Description

Brief Summary

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.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: phone call support
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
48 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Supportive Care
Official Title:
Phone Call as an Intervention for Improving Walking Practice in Type 2 Diabetes: Influence of Personality Profile in This Response
Study Start Date :
Jan 1, 2008
Actual Primary Completion Date :
Oct 1, 2008
Actual Study Completion Date :
Oct 1, 2008

Arms and Interventions

Arm Intervention/Treatment
Experimental: 1

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

Behavioral: phone call support
The intervention group received a phone call support for 6 weeks to incentive to increase the number of steps/day.
Other Names:
  • couselling to behavior change
  • No Intervention: 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.

    Outcome Measures

    Primary Outcome Measures

      Eligibility Criteria

      Criteria

      Ages Eligible for Study:
      40 Years and Older
      Sexes Eligible for Study:
      All
      Accepts Healthy Volunteers:
      No
      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

      Contacts and Locations

      Locations

      No locations specified.

      Sponsors and Collaborators

      • University of Sao Paulo

      Investigators

      None specified.

      Study Documents (Full-Text)

      None provided.

      More Information

      Publications

      None provided.
      Responsible Party:
      , ,
      ClinicalTrials.gov Identifier:
      NCT00810173
      Other Study ID Numbers:
      • Fonseca-Guedes
      First Posted:
      Dec 17, 2008
      Last Update Posted:
      Dec 17, 2008
      Last Verified:
      Dec 1, 2008

      Study Results

      No Results Posted as of Dec 17, 2008