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Self-administered acupressure for chronic severe functional constipation: a study protocol for a randomized controlled trial

Self-administered acupressure for chronic severe functional constipation: a study protocol for a randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2000004116
Enrollment
Unknown
Registered
2020-09-24
Start date
2021-07-01
Completion date
Unknown
Last updated
2023-02-20

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

Conditions

Functional Constipation

Interventions

Sponsors

The Third Affiliated Hospital of Zhejiang Chinese Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1) Satisfaction of Rome IV Criteria for FC; 2) Two or fewer mean weekly Rome IV Criteria for more than 3 months; 3) Age between 18 and 65 years; 4) No administration of rescue medicine (glycerol or sorbitol anal enema) 48 hours before the trial or any medication for constipation before enrollment for at least 2 weeks; 5) No administration of any other therapy for constipation, such as acupuncture, acupressure, or biofeedback therapy, and no participation in any other trial in the previous 3 months; 6) Documented consent to participate in the whole study.

Exclusion criteria

Exclusion criteria: 1) Constipation possibly caused by irritable bowel syndrome, or inflammatory or structural bowel diseases; 2) Constipation possibly caused by drugs or endocrine, metabolic, neurologic, or postoperative diseases; 3) Presence of tumors, severe cardiovascular, hepatic, renal diseases, or other severe diseases; 4) Inability to cooperate because of cognitive dysfunction, aphasia, mental disorders, or other illness; 5) Pregnant women, lactating women, or those who plan to get pregnant in the following 3 months; 6) Presence of abdominal aortic aneurysm or hepatosplenomegaly; 7) Skin lesions at the operating site of the acupoints.

Design outcomes

Primary

MeasureTime frame
the proportion of Complete spontaneous bowel movements more than or equal to 3 in week 3-10;

Secondary

MeasureTime frame
Straining severity scores;the proportion of Complete spontaneous bowel movements more than or equal to 3 in week 11-18;The Bristol Stool Form Scale;spontaneous bowel movements;Patient assessment of constipation quality of life (PAC-QOL);

Countries

China

Contacts

Public ContactFan Binghua

The Third Affiliated Hospital of Zhejiang Chinese Medical University

fanbinhua@sina.com+86 18958077807

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Feb 4, 2026