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The effect of yoga on chronic abdominal pain and quality of life.

Comparison of the effect of yoga and standard care on functional abdominal pain: Pain reduction and improvement of quality of life? A randomized controlled trial.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON21105
Enrollment
65
Registered
2012-02-14
Start date
2012-04-01
Completion date
Unknown
Last updated
2024-06-11

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

Conditions

chronic abdominal pain

Interventions

Yoga therapy will be given in groups of 7- 8 children per group, in which patients will receive one treatment session each week for 3 months. These hatha yoga sessions of 1.5 h each will be provided b

Sponsors

Jeroen Bosch hospital, Den Bosch
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Children aged 8-18 years are included if they meet the criteria for functional dyspepsia, IBS, functional abdominal pain (FAP) or abdominal migraine, based on the Rome III Criteria for Functional Bowel Disorders Associated with Abdominal Pain or Discomfort in Children.

Exclusion criteria

Exclusion criteria: Children with abdominal pain as result of inflammatory, anatomic, metabolic or neoplastic disease. Children who already participated in yoga therapy, hypnotherapy, psychotherapy or any form of relaxation therapy for functional abdominal pain in the past. Children with mental retardation.

Design outcomes

Primary

MeasureTime frame
The reduction of abdominale pain is our primairy outcome. Abdominale pain is measured by an abdominal pain diary. Patients will be instructed to score pain intensity and pain frequency during 1 month at baseline period, after finishing the treatment and at 6 and 12 months follow up. Clinical remission is defined as a decrease of the pain intensity score and pain frequency score of > 80%; significant improvement is defined as a decrease of pain intensity score and pain frequency score between 30% and 80% and treatment is considered unsuccessful if the scores improved < 30% or got worse.

Secondary

MeasureTime frame
Secondary outcome measure is the quality of life, which will be measured by the The Kidscreen-27 Quality of Life questionnaire. This questionnaire will be administered to the patients and their parents at baseline, after finishing the treatment and at 6 and 12 months follow up.

Contacts

Public ContactJ.J. Korterink

Postbus 90153

j.korterink@jbz.nl+31 (0)73 5337932

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)