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

S

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

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

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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