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Health Belief Model Nursing for Moderate to Severe OSAHS Post-Surgery

H

Hebei Medical University

Status

Completed

Conditions

Postoperative Care
Obstructive Sleep Apnea-Hypopnea Syndrome (OSAHS)

Treatments

Behavioral: Health Belief Model Nursing Intervention
Behavioral: Routine Care

Study type

Interventional

Funder types

Other

Identifiers

NCT07050602
20160703

Details and patient eligibility

About

This study aimed to investigate the long-term preventive and therapeutic effects of a health belief model (HBM)-based nursing intervention compared to routine care in patients with moderate to severe Obstructive Sleep Apnea-Hypopnea Syndrome (OSAHS) after surgery. The study assessed impacts on sleep parameters (Apnea-Hypopnea Index, Oxygen Desaturation Index, sleep quality via PSQI), self-management abilities, quality of life, OSAHS recurrence rate, and patient satisfaction.

Full description

A total of 120 post-surgery patients with moderate to severe OSAHS were recruited and assigned to either a control group (n=60) receiving routine postoperative care or an observation group (n=60) receiving a health belief model-based nursing intervention in addition to routine care. Routine care included general postoperative education for OSAHS, dietary, and exercise guidance with monthly phone follow-ups. The HBM intervention, lasting one year, focused on perceived susceptibility (assessment, psychological intervention), perceived severity (education on risks), perceived benefits (weight/BP monitoring, dietary/exercise guidance, sleep posture aids, daily diary), and perceived barriers (frequent phone follow-ups, psychological support). Outcomes were measured at baseline, 6 months, and 12 months post-surgery, including polysomnography, Pittsburgh Sleep Quality Index (PSQI), self-management ability questionnaires, quality of life questionnaires, OSAHS recurrence, and patient satisfaction surveys.

Enrollment

120 patients

Sex

All

Ages

30 to 50 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Aged between 30 and 50 years old;
  • Sleep Apnea Hypopnea Index (AHI) > 21 events per hour;
  • Body Mass Index (BMI) ≥ 28 kg/m²;
  • The obstructive plane of OSAHS was either at the soft palate level or associated with narrowing at the tongue base level;
  • Surgical treatments included uvulopalatopharyngoplasty (UPPP) or UPPP combined with low-temperature plasma ablation of the tongue base/tongue body;
  • The patient had undergone surgical treatment for OSAHS;
  • The patient could comprehend the research details and voluntarily signed an informed consent form.

Exclusion criteria

  • Severe cardiovascular disease, kidney disease, liver disease, or dysfunction of other major organs;
  • Severe mental illness or cognitive dysfunction that would hinder understanding or adherence to research procedures;
  • Presence of other sleep disorders, such as central sleep apnea or insomnia;
  • Use of medications that could interfere with sleep patterns;
  • Pregnancy or lactation;
  • Patients unwilling to provide informed consent for the study.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

120 participants in 2 patient groups

Observation Group
Experimental group
Description:
Participants received routine postoperative care plus a one-year health belief model nursing intervention. This included: comprehensive assessment and psychological interventions (Perceived Susceptibility); education on OSAHS risks and consequences (Perceived Severity); weekly weight/blood pressure monitoring, dietary/exercise guidance, sleep posture correction aids, and a daily health diary (Perceived Benefits); and regular phone follow-ups (2-3 times/week for 0-8 weeks post-discharge, bi-weekly up to 1 year) for support and addressing difficulties (Perceived Barriers).
Treatment:
Behavioral: Routine Care
Behavioral: Health Belief Model Nursing Intervention
Control Group
Active Comparator group
Description:
Participants received routine postoperative care for OSAHS for one year, including general education, dietary and exercise guidance. Post-discharge monitoring was conducted via monthly phone calls.
Treatment:
Behavioral: Routine Care

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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