Cameroon Mobile Phone SMS Trial (CAMPS)
![]() |
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. |
ClinicalTrials.gov Identifier: NCT01247181 |
Recruitment Status :
Completed
First Posted : November 24, 2010
Last Update Posted : September 8, 2011
|
- Study Details
- Tabular View
- No Results Posted
- Disclaimer
- How to Read a Study Record
Condition or disease | Intervention/treatment | Phase |
---|---|---|
Adherence HIV | Other: Mobile phone text message Other: Usual care | Not Applicable |
Study Type : | Interventional (Clinical Trial) |
Actual Enrollment : | 200 participants |
Allocation: | Randomized |
Intervention Model: | Parallel Assignment |
Masking: | Triple (Care Provider, Investigator, Outcomes Assessor) |
Primary Purpose: | Supportive Care |
Official Title: | Improving Adherence to HAART Using Mobile Phone Text Messages |
Study Start Date : | November 2010 |
Actual Primary Completion Date : | July 2011 |
Actual Study Completion Date : | July 2011 |
Arm | Intervention/treatment |
---|---|
Experimental: Mobile phone text message |
Other: Mobile phone text message
Weekly message with motivational content
Other Names:
|
Active Comparator: No Mobile phone text message
Usual care provided at clinic
|
Other: Usual care
Usual care provided at clinic
Other Name: Routine care |
- Adherence [ Time Frame: Change from baseline at 6 months ]Measured using the Visual Analogue Scale, Self Report and Pharmacy Refill Data
- Weight [ Time Frame: Change from baseline at 6 months ]
- Body Mass Index [ Time Frame: Change from baseline at 6 months ]
- CDC classification [ Time Frame: Change from baseline at 6 months ]
- WHO Classification [ Time Frame: Change from baseline at 6 months ]
- Mortality [ Time Frame: 6 months ]All cause mortality
- CD4 count [ Time Frame: Change from baseline at 6 months ]
- Viral load [ Time Frame: Change from baseline at 6 months ]
- Quality of life [ Time Frame: Change from baseline at 6 months ]Measured using the SF-12 quality of life form

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
Ages Eligible for Study: | 21 Years to 65 Years (Adult, Older Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- On HAART for at least 1 month
- 21 years or more
- Owns a mobile phone
- Can read text messages
Exclusion Criteria:
- On HAART for less than 1 month
- Aged less than 21 years

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01247181
Cameroon | |
Yaounde Central Hospital Accredited Treatment Centre | |
Yaounde, Centre, Cameroon |
Principal Investigator: | Lawrence Mbuagbaw, MD, MPH | Centre for the Development of Best Practices in Health | |
Study Director: | Pierre Ongolo-Zogo, MD, BSc | Centre for the Development of Best Practices in Health |
Responsible Party: | Lawrence Mbuagbaw, MD, MPH, Yaounde Central Hospital |
ClinicalTrials.gov Identifier: | NCT01247181 |
Other Study ID Numbers: |
CAMPS PACTR201011000261458 ( Registry Identifier: Pan-African Clinical Trials Registry ) |
First Posted: | November 24, 2010 Key Record Dates |
Last Update Posted: | September 8, 2011 |
Last Verified: | September 2011 |
compliance observance mobile phone SMS |
text message ARV HAART AIDS |