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Controlled Outcome Evaluations of a Daily Physical Activity Intervention for Individuals With Type 2 Diabetes

U

University Ghent

Status

Completed

Conditions

Type 2 Diabetes

Treatments

Behavioral: Daily physical activity, pedometer and counseling

Study type

Interventional

Funder types

Other

Identifiers

NCT00903500
2005/380

Details and patient eligibility

About

The intervention consists of an individual counseling session, telephone counseling (7 calls), given by a psychologist, and a pedometer. The intervention is based on cognitive behavioral therapy, the Diabetes Prevention Program, the first Step Program and Motivational Interviewing. The taxonomy of behavior change techniques is also taken into account. The duration of the intervention is six months. The individual session takes place one week after the baseline measurements, together with the participants' follow-up appointment with their endocrinologist. The individual session takes place at the endocrinology department and is expected to last approximately 30 minutes. In addition to the session, the participants of the intervention group receive a pedometer and a pedometer diary for six months. Participants of the intervention group also receive telephone counseling from the psychologist during 24 weeks. They receive a call every two weeks for four weeks and then every four weeks for the next 20 weeks, good for a total of seven counseling calls. The calls are expected to last approximately 20 minutes. The Control Group has no intervention at all and receive their usual care.

Enrollment

92 patients

Sex

All

Ages

35 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  • Minimum six months post-diagnosis of type 2 diabetes age between 35 and 75 years
  • Treated by diet alone, oral hypoglycaemic medications, insulin or combination therapy
  • No documented PA limitations
  • Dutch speaking
  • Having a telephone number

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

92 participants in 2 patient groups

1
Experimental group
Description:
Daily physical activity
Treatment:
Behavioral: Daily physical activity, pedometer and counseling
2
No Intervention group
Description:
Usual care

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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