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Efficacy of 8 vs 4 Sessions Mindfulness-based Programs in a Non-clinical Population

U

University Hospital Miguel Servet

Status and phase

Completed
Early Phase 1

Conditions

Healthy Subjects

Treatments

Behavioral: 4-week shortened MBSR
Behavioral: standard 8-weeks MBSR

Study type

Interventional

Funder types

Other

Identifiers

NCT02643927
PI12/00134

Details and patient eligibility

About

The aim of this study was to assess and compare the efficacy of a standard 8-weeks protocol based on the Mindfulness Based Stress Reduction MBSR program versus a 4-week shortened version of the protocol in the improvement of wellbeing variables in a non-clinical population in Spain. The investigators initial hypothesis was that both protocols are efficacious but the standard 8-week performs better that the short one.

Enrollment

99 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • be adult (18-y or older);
  • willingness to participate in the study and signing informed consent;
  • ability to understand and write Spanish.

Exclusion criteria

  • have an acute clinical or psychiatry condition;
  • have no previous experience with mindfulness or other type of contemplative or mind-boy practices such as yoga, taichi or chikung.

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Factorial Assignment

Masking

Double Blind

99 participants in 3 patient groups

standard 8-weeks MBSR
Experimental group
Description:
8-week program
Treatment:
Behavioral: standard 8-weeks MBSR
4-week shortened MBSR
Experimental group
Description:
Short 4 sessions intervention
Treatment:
Behavioral: 4-week shortened MBSR
Control Group
No Intervention group
Description:
control group: No intervention

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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