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Application of an Activity Pacing Intervention Program in Patients with Brucellosis

Application of an Activity Pacing Intervention Program in Patients with Brucellosis

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600117541
Enrollment
Unknown
Registered
2026-01-26
Start date
2026-01-30
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

Brucellosis

Interventions

Intervention group:In addition to routine nursing care provided in the Brucellosis Department, patients receive an intervention program focused on activity rhythm adjustment, including: 1. Baseline ac
2. Education on activity rhythm adjustment (second week after discharge, consisting of two sessions)
3. Implementation of the activity rhythm adjustment plan (weeks 3–6 after discharge, consisting of two sessions)
4. Review of learned content and long-term planning (seventh and nineteenth weeks after discharge). The intervention is delivered via online platforms such as Tencent Meeting and WeChat, and includes
Control group:Participants received conventional care and follow-up services provided by the outpatient and inpatient departments of the Brucellosis Clinic at Inner Mongolia International Mongolian Ho

Sponsors

No. 2 Hospital of Hohhot
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Diagnosis of brucellosis confirmed according to the Guidelines for the Diagnosis and Treatment of Brucellosis (Trial), evidenced by relevant clinical manifestations and positive immunological tests, and absence of other severe comorbidities; 2. Age 18 years or older; 3.Demonstrated ability to use a sports watch and the WeChat application following a structured orientation; 4.Provision of informed consent to participate in the study.

Exclusion criteria

Exclusion criteria: 1. Presence of severe comorbidities and/or communication barriers. 2. Asymptomatic individuals. 3. Identification of an adapted pacing pattern as assessed by the Pain-Related Activity Patterns Scale. 4. Concurrent participation in other interventional research studies.

Design outcomes

Primary

MeasureTime frame
Quality of Life;Depression;Anxiety;Patterns of Activity;Symptom Cluster;Physical Activity;

Countries

China

Contacts

Public ContactWen Qi

No. 2 Hospital of Hohhot

460389787@qq.com+86 138 4814 0444

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 7, 2026