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The effectiveness of acceptance and commitment intervention for chronic postsurgical pain in patients undergoing hysterectomy due to benign causes: a randomized controlled trial

The effectiveness of acceptance and commitment intervention for chronic postsurgical pain in patients undergoing hysterectomy due to benign causes: a randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200056593
Enrollment
Unknown
Registered
2022-02-08
Start date
2022-03-01
Completion date
Unknown
Last updated
2024-10-21

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

Conditions

Benign gynecological disease for which total hysterectomy is planned

Interventions

ACT group:Acceptance and commitment therapy + usual care
UC group:Usual care

Sponsors

Sichuan Academy of Medical Sciences & Sichuan Provincial People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Women scheduled for total hysterectomy due to benign disease; 2. Patients aged 18 years or older with informed consent; 3. Previous history of cesarean section or chronic pain three months before surgery (NRS>=3) or hospital Anxiety and Depression scale >=8 or pain Catastrophization scale >=30.

Exclusion criteria

Exclusion criteria: 1. Currently participating in pain psychological treatment; 2. Have a serious health condition that may prevent participation; 3. Bipolar disorder or mental disorder, history of brain injury; 4. Unable to complete the study form due to language barrier or other factors; 5. Imminent risk of suicide; 6. Participated in ACT or mindfulness therapy in the previous year.

Design outcomes

Primary

MeasureTime frame
Pain;Effects of pain on physical function;Reporting of adverse events;

Secondary

MeasureTime frame
Use of postoperative analgesics;Difference of NRS score > 3 between the two groups at 3 months after operation;General health status ;Satisfaction with the intervention in the ACT group;Use of analgesics after discharge;

Countries

China

Contacts

Public ContactLiao Limei; Xia Xueqin

Sichuan Academy of Medical Sciences & Sichuan Provincial People's Hospital

limeiliao@uestc.edu.cn+86 15184455326

Outcome results

None listed

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