NCT07076667

Brief Summary

Chronic Obstructive Pulmonary Disease (COPD) is a progressive lung disorder that significantly impacts respiratory function and quality of life. As COPD patients often experience symptoms such as dyspnea, fatigue, and anxiety, non-pharmacological interventions like Benson's Relaxation Technique and Tai Chi are gaining attention for their potential benefits in managing these symptoms.This study aimed to compare the effectiveness of Benson's Relaxation Technique and Tai Chi on improving dyspnea, physical endurance, and quality of life in COPD patients.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
54

participants targeted

Target at P25-P50 for not_applicable

Timeline
8mo left

Started Jul 2025

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress57%
Jul 2025Dec 2026

First Submitted

Initial submission to the registry

July 3, 2025

Completed
Same day until next milestone

Study Start

First participant enrolled

July 3, 2025

Completed
19 days until next milestone

First Posted

Study publicly available on registry

July 22, 2025

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 15, 2025

Completed
1.1 years until next milestone

Study Completion

Last participant's last visit for all outcomes

December 25, 2026

Expected
Last Updated

July 22, 2025

Status Verified

July 1, 2025

Enrollment Period

5 months

First QC Date

July 3, 2025

Last Update Submit

July 21, 2025

Conditions

Keywords

Benson relaxation techniqueTai ChiPulmonary rehabilitation

Outcome Measures

Primary Outcomes (3)

  • MODIFIED BORG DYSPNEA SCALE

    The MBS is a valid and reliable assessment tool for dyspnea. It is a tool to assess and rate the difficulty in breathing (dyspnea) rated from 0 to 10. 0 shows no dyspnea whereas 10 shows max dyspnea.

    8 weeks

  • SIX MINUTE WALK TEST

    The 6 MWT is safe,easy to administer,better tolerated, and reflects activities of daily living.When conducting the 6MWT do not walk with the patient and do not assist the patient in carrying or pulling his or her supplemental oxygen.The patient should walk alone,not with other patients.Do not use an oval or circular track. Use standardized phrases while speaking to the patient, because your encouragement and enthusiasm can make a difference of upto 30% in the 6MWD.Count the laps with a lap counter.

    8 weeks

  • SPIROMETER

    Spirometers arei nstruments to conduct spirometry tests.Earlier,spirometers were of either rolling model or bellows type but the recent ones are electronic and fully automated using digital turbine and flow sensors that require no calibration. Though spirometry does not measure the individual lung volumes,it measures the forced vital capacity (FVC).

    8 weeks

Secondary Outcomes (1)

  • St.GEORGE'S RESPIRATORY QUESTIONNAIRE

    8 weeks

Study Arms (2)

Benson'srelaxationtechnique

ACTIVE COMPARATOR

"Benson's Relaxation Technique"along with the standard COPD care and medication.

Other: Benson's relaxation technique

TaiChi

EXPERIMENTAL

"Tai Chi relaxation Technique" along with the standard COPD care and medication

Other: Tai Chi

Interventions

effects of Benson's relaxation technique 5 days per week for 45 minutes for 8 weeks

Benson'srelaxationtechnique
Tai ChiOTHER

Tai Chi 5 days per week for 45 minutes for 8 weeks

TaiChi

Eligibility Criteria

Age40 Years - 50 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • Age40 to 50
  • Bothmaleandfemale
  • DiagnosedmoderatetosevereCOPDpatients
  • Participants must be physicallyable to participate in Tai Chi or Benson relaxation technique
  • Participantsmustbewillingtoparticipate

You may not qualify if:

  • Pulmonaryhypertension
  • Congenitalheartdisease(recentmyocardialinfarction,unstableangina,or uncontrolled hypertension)
  • Spinal deformities
  • Lossof consciousness

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Bahawalpur Victoria Hospital

Chak Four Hundred Fifty-four, Punjab Province, 63100, Pakistan

RECRUITING

Related Publications (5)

  • Cavailles A, Brinchault-Rabin G, Dixmier A, Goupil F, Gut-Gobert C, Marchand-Adam S, Meurice JC, Morel H, Person-Tacnet C, Leroyer C, Diot P. Comorbidities of COPD. Eur Respir Rev. 2013 Dec;22(130):454-75. doi: 10.1183/09059180.00008612.

    PMID: 24293462BACKGROUND
  • 2. LeungJM,ObeidatMe,SadatsafaviM,SinDD.Introductiontoprecisionmedicinein COPD. European Respiratory Journal. 2019;53(4).

    BACKGROUND
  • 3. AgustíA,VogelmeierC,FanerR.COPD2020:changesandchallenges.American Physiological Society Bethesda, MD; 2020. p. L879-L83.

    BACKGROUND
  • Nazari AM, Zare-Kaseb A, Arbabi Z, Gholampour MH, Emami Zeydi A, Ghazanfari MJ. The effect of Benson relaxation technique on cancer patients: a systematic review. Support Care Cancer. 2023 Nov 8;31(12):681. doi: 10.1007/s00520-023-08142-2.

    PMID: 37938356BACKGROUND
  • JonesP,QuirkF,BaveystockC.TheStGeorge'sRespiratoryQuestionnaire.Respiratory medicine. 1991;85:25-31; discussion 3

    BACKGROUND

MeSH Terms

Conditions

Pulmonary Disease, Chronic Obstructive

Interventions

Tai Ji

Condition Hierarchy (Ancestors)

Lung Diseases, ObstructiveLung DiseasesRespiratory Tract DiseasesChronic DiseaseDisease AttributesPathologic ProcessesPathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

Mind-Body TherapiesComplementary TherapiesTherapeuticsExercise Movement TechniquesPhysical Therapy Modalities

Study Officials

  • Iram Nawaz, Mphill

    Riphah International University

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

July 3, 2025

First Posted

July 22, 2025

Study Start

July 3, 2025

Primary Completion

November 15, 2025

Study Completion (Estimated)

December 25, 2026

Last Updated

July 22, 2025

Record last verified: 2025-07

Data Sharing

IPD Sharing
Will not share

Locations