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Additional Effects of Quranic Listening Meditation in Combination With High Intensity Interval Training in Obese Adults

R

Riphah International University

Status

Completed

Conditions

Obesity

Treatments

Other: High Intensity interval training + Quranic Listening
Other: High intensity interval training

Study type

Interventional

Funder types

Other

Identifiers

NCT06442371
Rec/01809 Warda Zaman

Details and patient eligibility

About

To determine the additional effects of Quranic listening meditation, in combination with High-Intensity Interval Training on cardiovascular fitness and mental health in obese adults.

Enrollment

52 patients

Sex

All

Ages

18 to 45 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Obese adults (BMI ≥ 30)
  • Age range: 18-45 years
  • No previous experience with Quranic listening meditation since last 4 weeks.
  • No contraindications for engaging in high-intensity physical activity
  • Able to attend regular sessions at clinic and follow the study protocol.
  • Willingness to undergo pre and post-assessments for cardiovascular fitness and mental health measures.

Exclusion criteria

  • Individuals with a history of the medical condition being studied
  • Those who are currently taking medication that may affect the study
  • Participants with a history of mental health disorders
  • Individuals who are pregnant or breastfeeding
  • Those who have previously participated in a similar study
  • Participants with a history of substance abuse or addiction

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

52 participants in 2 patient groups

High Intensity interval training + Quranic Listening
Experimental group
Treatment:
Other: High Intensity interval training + Quranic Listening
High Intensity interval training
Active Comparator group
Treatment:
Other: High intensity interval training

Trial contacts and locations

1

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Central trial contact

Muhammad Iqbal Tariq, PhD*

Data sourced from clinicaltrials.gov

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