A randomized controlled trial of cognitive behavioral therapy-based self-monitoring for irritable bowel syndrome in female nursing school students

A randomized controlled trial of cognitive behavioral therapy-based self-monitoring for irritable bowel syndrome in female nursing school students - Self-monitoring for irritable bowel syndrome

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000011436

Enrollment

103

Registered

2013-08-09

Start date

2009-06-01

Completion date

Unknown

Last updated

2026-06-29

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

Conditions

Irritable bowel syndrome (IBS)

Interventions

The intervention groups conducted lifestyle self-monitoring in conjunction with a 15-minutes group work for two months. The intervention groups conducted lifestyle self-monitoring in conjunction with

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: females no diagnosis of inflammatory bowel diseases data inadequacy

Exclusion criteria

Exclusion criteria: males diagnosis of inflammatory bowel diseases no data inadequacy

Design outcomes

Primary

Measure	Time frame
The primary outcome measures were Rome II criteria for IBS, the Hospital Anxiety and Depression Scale (HADS) and the Gastrointestinal Symptom Rating Scale (GSRS), assessed at the baseline and the end of both of the intervention periods.	—

Countries

Japan

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026