Effectiveness of Mobile Phone-Based Intervention to Prevent Smoking Relapse Among Recent Smoking Quitters

Smoking Cessation Clinical Trial

Official title:

Effectiveness of Mobile Phone-Based Intervention to Prevent Smoking Relapse Among Recent Smoking Quitters in Jazan Region: Randomized Control Trial.

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT03994445
• Other study ID #: SRP in recently quit smokers
• Status: Not yet recruiting
• Phase: N/A
• Start date: July 1, 2019
• Est. completion date: April 30, 2020

Study information

• Verified date: June 2019
• Source: King Khalid University
• Contact: Ibtihal Altalhi, MBBS
• Phone: 955540072443
• Email: ebtihal2012[@]hotmail.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Main Objective The main objective of the study is to investigate the effectiveness of a mobile phone-based intervention in reducing relapse ate among recent quitters who are attending the smoking cessation program in Jazan.

Besides this, the study will achieve the following objective:

To identify the timing and different factors associated with relapse process among recent quitters during first 6 months of quitting.

Description:

Background:

Smoking remains a major public health problem and an important cause of morbidity and mortality worldwide. Although the effectiveness of behavior support and medical treatment, many of those who quit smoking subsequently relapse to smoke.

Objective:

The primary aim of this study will be to determine the effectiveness of the mobile phone-based intervention to prevent relapse among recent smoking quitters. Also, the study aims to identify the different factors associated with relapse among recent quitters during the first 6 months of quitting.

Design and Methods:

A parallel two-armed Randomized Controlled Trial (RCT) to assess the effectiveness of a mobile phone-based intervention for smoking cessation on achieving long term abstinence, will be conducted among volunteers. Participants will be recruited from those attended smoking cessation program in Southern Alrawdha clinic, Southern Abo Arish clinic, Sabia clinic and Aldhabia clinic.

Primary outcome:

The difference in relapsing rate among recent quitters, which may subsequently contribute in to a reduction in smoking rates.

Trail Implications for public Health:

The result of this study will provide evidence for effectiveness of the mobile phone-based intervention versus standard treatment to reduce smoking relapse rate. If proven, it will be a cost-saving intervention by reducing repeat use of the smoking cessation clinic services and by reducing use of healthcare services for smoking-related illness.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 476
• Est. completion date: April 30, 2020
• Est. primary completion date: March 31, 2020
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 65 Years

Eligibility

Inclusion Criteria:

• Aged 18 years or older.

• Recent quitters (24 hours smoking abstinence)

• Willing to provide informed consent to participate in the study.

Exclusion Criteria:

• Those suffering any physical or mental disorders.

• Illiterate people.

• Pregnant.

Related Conditions & MeSH terms

• Smoking Cessation

Intervention

Behavioral:
• Mobile Phone-Based Intervention
We propose our intervention based on social cognitive behavior theories and the stages of the change model. The program will be carried out using the word "Mettle", it will help ex-smokers stay off cigarettes through advices generated to promote the health from religious concepts and culture perspectives .

Locations

Country	Name	City	State
Saudi Arabia	Smoking Cessation Clinic - Ministry of Health	Jazan

Sponsors (1)

Lead Sponsor	Collaborator
Ibtihal Altalhi

Country where clinical trial is conducted

Saudi Arabia, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	The primary study outcome will be the difference at 6 months relapse rate between the two arms, relapse rate will be identified as a return to continuous smoking even a puff after obtaining 24 hours of abstinence	Relapse rates at the end of the 3rd and 6th month of follow-up in the intervention and control groups.	6 months following scheduled quit date
Secondary	Secondary outcomes included: (1) timing till self-reported relapse. (2) causes of relapse.	Participants will be asked core smoking status questions, including whether they have smoked any cigarettes or used other tobacco products, even a puff, in the last 30 days, 7-day point prevalence abstinence, the exact day of each smoking relapse episode and the cause of relapse.	6 months following scheduled quit date