IBSR Intervention for Adults Who Stutter

Tel Aviv Sourasky Medical Center

Status: Completed

Conditions: Stuttering

Treatments: Behavioral: Inquiry Based Stress Reduction (IBSR) workshop

Study type: Interventional

Funder types: Other

Identifiers

NCT04580966

IBSR-Stuttering

Details and patient eligibility

About

Stuttering is a speech disorder that can cause disturbances in the timing and flow of speech. It is often accompanied not only by verbal difficulties but also by negative impact on several psycho-social aspects in the life of the people who stutter.

Recently, clinical evidences have shown the effectiveness of Inquiry Based Stress Reduction (IBSR) technique to improve psychosocial symptoms and enhance well-being in clinical and non-clinical samples. IBSR, the clinical application of Byron Katie's "The Work", enables individuals to mindfully spot and investigate in a systematic and comprehensive manner thoughts that lead to stress and suffering by a series of questions and turnarounds. IBSR was found to have significantly positive influence on the quality of life, mental well-being and stress management in a variety of populations which suffer from elevated levels of stress, suffering, tension and anxiety, and to enhance resilience of non-clinical general population.

In our research we hypothesized that:

1. Adults who stutter will have high levels of anxiety, and low levels of psychological flexibility and satisfaction with life.
2. IBSR intervention will improve experience of stuttering in adults who stutter.
3. IBSR will decrease anxiety levels and enhance psychological flexibility and satisfaction with life.

Enrollment: 56 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Diagnosis of either developmental or acquired stuttering.
• Age of 18 years or above.
• Capability to understand and fill out the study outcome instruments and informed consent form.

Exclusion criteria

• Diagnosis of severe mental illness.
• Inability to understand or read Hebrew.
• Subjects who declare they can not take a part in the trial throughout its whole duration.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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56 participants in 2 patient groups

Inquiry Based Stress Reduction (IBSR) workshop

Experimental group

Description:

Participants of this group received an IBSR intervention workshop.

Treatment:

Behavioral: Inquiry Based Stress Reduction (IBSR) workshop

Control group

No Intervention group

Description:

Participants of this group did not take a part in the workshop.