ClinicalTrials.Veeva

Menu

A Tailored Feasibility Study to Increase Physical Activity and to Reduce Sedentary Time

U

University Medicine Greifswald

Status

Completed

Conditions

Cardiovascular Risk Factor

Treatments

Behavioral: Counseling letter

Study type

Interventional

Funder types

Other

Identifiers

NCT02990039
FKZ 81Z5400152

Details and patient eligibility

About

The purpose of this study was (i) to develop a brief counseling letter intervention aiming to reduce sedentary time and to increase physical activity during leisure time among adults aged 42 to 64 years and (ii) to provide information on the feasibility.

Full description

The study aimed to assess the feasibility of a brief counseling letter intervention to increase physical activity and to reduce sedentary time in leisure time.

Following the Intervention Mapping Protocol we developed the counseling letter intervention. The intervention is based on the Health Action Process Approach, comprising 3 tailored letters based on separate assessments, delivered over 6 month.

All participants consented (i) to participate in an examination at the university hospital including standardized measurements of blood pressure, waist and hip circumference, body height and weight as well as blood sample taking, (ii) to fill in a paper-pencil questionnaire, and (iii) to wear an accelerometer for 7 days at baseline and at 12-month follow-up.

A general population sample of cardiovascular healthy adults was randomly allocated to a control and an intervention group. At 5 time points (baseline, 3-month, 6-month, 7-month, and 12-month follow-up) participants of both study groups completed standardized questionnaires.

Enrollment

176 patients

Sex

All

Ages

42 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • age between 42 and 65 years
  • resident in a pre-defined zip-code area

Exclusion criteria

  • cardiovascular event (myocardial infarction, stroke) or vascular intervention
  • self-reported body-mass-index over 35 kg/m²

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

176 participants in 2 patient groups

Counseling letter (intervention group)
Experimental group
Description:
Participants of the intervention group received a brief counseling letter intervention aiming to reduce sedentary time and to increase physical activity. The intervention comprised up to three tailored letters based on separate questionnaires.
Treatment:
Behavioral: Counseling letter
No counseling letter (control group)
No Intervention group
Description:
Participants of the control group did not received the brief counseling letter intervention.

Trial contacts and locations

0

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems