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A Stress Reduction Program for Companies

A Randomized Controlled Trial With a Follow-up Evaluation of a Stress Reduction Program for Companies - PROGRESS

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02660307
Enrollment
41
Registered
2016-01-21
Start date
2014-02-28
Completion date
2014-09-30
Last updated
2018-05-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stress

Keywords

stress, work, employees, mindfulness, depression, anxiety

Brief summary

This protocol proposes a well-being program based in stress reduction program for employees of a company. objectives: To evaluate the effects of a stress reduction program with a specific orientation for workers and taught to them within their companies. Methods: Participants with stress complaints were recruited and randomized into two groups: group 1 (G1) received the intervention while group 2 (G2) did not. Both groups were evaluated before the intervention (time 1 - T1); again after the eight weeks of the program for G1 (time 2 - T2); and then at the end of a second eight-week period during which G2 received the intervention and G1 was simply instructed to maintain the practice they had learned without further instruction (time 3- T3).

Detailed description

Disorders resulting from chronic stress are some of the main causes of absenteeism and reduced productivity in companies. A number of successful stress management programs are based on the principle of mindfulness and may help individuals to relieve stress symptoms and to improve well-being and pro-social behavior. The objective of this study was to evaluate the feasibility and efficacy of a weekly one-hour stress reduction program adapted for companies and if the possible benefits would be sustained 8 weeks after the end of the program. Participants with stress complaints were recruited in two companies and they were randomized into two groups: in the first period of the study, group 1 (G1) N=23 received the intervention while group 2 (G2) N=18 did not. Both groups were evaluated before the intervention (time 1 - T1); again after the eight weeks of the program for G1 (time 2 - T2); and then at the end of a second eight-week period during which G2 received the intervention and G1 was simply instructed to maintain the practice they had learned without further instruction (time 3- T3).

Interventions

OTHERPROGRESS group

Sponsors

SESI (Serviço Social da Indústria)
CollaboratorUNKNOWN
Centro de estudos em Atenção Plena
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

* workers with stress complaints aging from 18 to 60 years. They also had to have at least 8 years of education.

Exclusion criteria

* participants with a history of psychiatric or neurological disorders or who were under psychological or psychiatric treatment during the period of the study, or with a history of substance abuse, with the exception of tobacco.

Design outcomes

Primary

MeasureTime frameDescription
changes in subjective symptoms of stressbaseline, 8 weeks and 16 weeksquestionnaire for stress symptoms via 37 somatic symptoms and 19 psychological symptoms.

Secondary

MeasureTime frameDescription
changes in subjective depression symptomsbaseline, 8 weeks and 16 weeksquestionnaire for depression symptoms, 21 items describing depression symptoms, each item in a scale from 0 to 3.
changes in anxiety symptomsbaseline, 8 weeks and 16 weeksquestionnaire for anxiety symptoms, 21 items describing anxiety symptom, each item in a scale from 0 to 3.
changes in speed of perception and visual and motor responsebaseline, 8 weeks and 16 weeksthis test is the association of numbers and symbols lasting 2 minutes. This variable measure is a neuropsychological test and the data presentation are in total scores
changes in Mindful Awareness and attentionbaseline, 8 weeks and 16 weeksin a scale from 1 to 6 the participant classifies how frequently or infrequently he/she becomes aware or mindful by contemplating the 15 described daily conditions provided
changes in psychiatric symptomsbaseline, 8 weeks and 16 weeksquestionnaire for psychiatric symptoms with 20 questions about mental health

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 24, 2026