Clinical Effectiveness of Combining Mindfulness-Based Stress Reduction With Exercise Interventione

Shanxi Bethune Hospital

Status: Completed

Conditions: Non-Small Cell Lung Cancer

Treatments: Behavioral: routine health education; Behavioral: MBSR therapy; Behavioral: exercise therapy; Behavioral: psychological nursing

Study type: Interventional

Funder types: Other

Identifiers

NCT06224504

SBH-001

Details and patient eligibility

About

This study is to assess the clinical effectiveness of combining Mindfulness-Based Stress Reduction (MBSR) with exercise intervention in improving anxiety, depression, sleep quality, and mood regulation in Chinese patients with non-small cell lung cancer (NSCLC).The control group received conventional psychological nursing care, while the intervention group received a combination of MBSR and exercise therapy. Pre- and post-treatment scores of anxiety, depression, sleep quality, and the BSRS-5 were compared.

Full description

To assess the clinical effectiveness of combining Mindfulness-Based Stress Reduction (MBSR) with exercise intervention in improving anxiety, depression, sleep quality, and mood regulation in Chinese patients with non-small cell lung cancer (NSCLC). A total of 60 lung cancer patients from a hospital in Shanxi Province were selected using convenience sampling and divided into an intervention group and a control group, with 30 patients in each group. The control group received conventional psychological nursing care, while the intervention group received a combination of MBSR and exercise therapy. The two group were evaluated by the questionnaire three times. One day before the intervention, the first questionnaire was conducted, and the basic data of the two groups of patients were collected. The second questionnaire evaluation of anxiety, depression, sleep quality, and the Brief Symptom Rating Scale (BSRS-5) was conducted 6 weeks after the end of the intervention, and the third questionnaire evaluation was conducted 8 weeks after the end of the intervention to evaluate the intervention effect of the two groups. Pre- and post-treatment scores of anxiety, depression, sleep quality, and the BSRS-5 were compared.

Enrollment: 60 patients

Sex: All

Ages: 44 to 65 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• patients diagnosed with non-small cell lung cancer
• patients aged between 20 and 74 years, without gender limitation
• a score of 4-14 on the Short Symptom Rating Scale (BSRS-5)
• a clinical prognosis of at least 6 months
• clear consciousness, good functional ability, and unrestricted language communication
• written informed consent provided by the patient

Exclusion criteria

• patients with severe physical illnesses or symptoms that impede learning and are considered life-threatening
• patients with a BSRS-5 assessment score > 15 and suicidal ideation > 2
• patients unable to accurately describe their symptoms
• patients with limited cooperation ability
• patients who have previously undergone MBSR or other positive-thinking-focused psychotherapy methods

Trial design

Primary purpose: Supportive Care

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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60 participants in 2 patient groups

the intervention group

Experimental group

Description:

routine health education ， psychological nursing， MBSR therapy ， exercise therapy

Treatment:

Behavioral: psychological nursing

Behavioral: exercise therapy

Behavioral: MBSR therapy

Behavioral: routine health education

the control group

Active Comparator group

Description:

routine health education ， psychological nursing

Treatment:

Behavioral: psychological nursing

Behavioral: routine health education